Postdoctoral Research Associate
University of Technology Sydney · Posted today
About the role
, defence and space. We are seeking to engage a Postdoctoral Research Associate for a period of up to 15-months...'s most liveable cities. With a culturally diverse campus life and extensive international exchange and research programs, UTS prepares
Research Assistant/Associate
The University of Newcastle · Posted today
About the role
Salary: Research Assistant: £34,630 to £36,320 per annum Research Associate: £37,369 to £46,970 per annum... The Role We are excited to offer an opportunity for a Research Assistant/ Associate in Neuromuscular Diseases
Research Assistant/Associate in Sustainable Carbon-Based Electrodes for Flow Batteries
The University of Newcastle · Posted today
About the role
Salary: Research Assistant: £34,630 to £36,320 per annum Research Associate: £37,369 to £41,885 per annum... The Role We are seeking an enthusiastic Research Assistant/Associate to join an exciting Innovate UK-funded feasibility
Clinical Research Associate II
ICON · Posted 1 days ago
About the role
Clinical Research Associate, Home-based in Australia ICON is a global healthcare intelligence and clinical research... to join our diverse and dynamic team. As a Clinical Research Associate at ICON, you will play a pivotal role in designing and analyzing
Senior/Clinical Research Associate
IQVIA · Posted 1 days ago
About the role
Are you a (Senior) Clinical Research Associate looking for your next big adventure? Look no further than IQVIA... be accepted in lieu of degree. Good knowledge of, and skill in applying, applicable clinical research regulatory requirements
Research Associate in Land Systems Science
The University of Newcastle · Posted 1 days ago
About the role
you. Closing Date: 11 November 2026 The Role We are excited to launch this new opportunity for a Research Associate in Land.... You will work closely with another Research Associate on the project, whose focus will be on biodiversity functions and connectivity
Senior Clinical Research Associate (Brisbane)
Thermo Fisher Scientific · Posted 1 days ago
About the role
find cures for cancer. About the Role: Join Us as a Senior Clinical Research Associate (Level I or II) – Make an Impact..., and abilities to perform the job (comparable to 3+ years as a clinical research monitor). In some cases an equivalency, consisting
Senior/Clinical Research Associate
IQVIA · Posted 1 days ago
About the role
Are you a (Senior) Clinical Research Associate looking for your next big adventure? Look no further than IQVIA... be accepted in lieu of degree. Good knowledge of, and skill in applying, applicable clinical research regulatory requirements
Inhouse Clinical Research Associate - Australia
Novotech · Posted 1 days ago
About the role
Job Description: The Inhouse Clinical Research Associate (IHCRA) provides in-house support to the clinical team... Contract Research Organization (CRO). At Novotech, ambition meets opportunity. As a globally recognized leader in clinical
Clinical Research Associate (Level I or II)
Thermo Fisher Scientific · Posted 1 days ago
About the role
all aspects of the clinical monitoring and site management process. As a Clinical Research Associate (Level I), you'll conduct... research monitor) or completion of PPD Drug Development Fellowship. In some cases an equivalency, consisting
Senior Clinical Research Associate (Melbourne or Sydney)
Thermo Fisher Scientific · Posted 1 days ago
About the role
find cures for cancer. About the Role: Join Us as a Senior Clinical Research Associate (Level II) – Make an Impact at the... that provides the knowledge, skills, and abilities to perform the job (comparable to 3+ years as a clinical research monitor
Senior Clinical Research Associate II (Perth or Adelaide)
Thermo Fisher Scientific · Posted 1 days ago
About the role
find cures for cancer. About the Role: Join Us as a Senior Clinical Research Associate (Level II) – Make an Impact at the... that provides the knowledge, skills, and abilities to perform the job (comparable to 3+ years as a clinical research monitor
Clinical Research Associate II/III - NSW
Novotech · Posted 2 days ago
About the role
Requisition Type Standard Requisition Number 4490 Requisition Title Clinical Research Associate II/III - Sydney... Duration Months Posting description InternalExternal Short Description Description The Clinical Research Associate
Senior Clinical Research Associate - NSW
Novotech · Posted 2 days ago
About the role
Job Description: The Clinical Research Associate (CRA), is primarily responsible for ensuring the rights.... collaboration with the In-house Clinical Research Associate (IHCRA) and Regulatory Start Up Associate (RSA), prepare site essential
Senior Clinical Research Associate
ICON · Posted 3 days ago
About the role
Senior Clinical Research Associate - Phase I, Onc- NSW/VIC At ICON Strategic Solutions, you will work in a sponsor... scientific discipline or healthcare-related field Extensive experience as a Clinical Research Associate, with a strong
Research Associate in Imaging in NMDs
The University of Newcastle · Posted 3 days ago
About the role
Associate (Evaluator) to our team at the John Walton Muscular Dystrophy Research Centre, Newcastle University, working... you. Closing Date: 09 November 2026 The Role We are delighted to offer an exciting opportunity for a Post Doctoral Research
Research Associate - Chemistry
UNSW Fitness and Aquatic Centre Management · Posted 4 days ago
About the role
in First Year, Synthetic, Analytical and Physical Chemistry. The Research Associate contributes to research... (35 hours per week) The role of Research Associate reports to Scientia Professor Justin Gooding and has no direct
Research Associate- School of Photovoltaic and Renewable Energy Engineering
UNSW Fitness and Aquatic Centre Management · Posted 7 days ago
About the role
following link: Position Summary: The Research Associate (Level A) contributes to UNSW's research excellence through the... collaboratively with researchers and academic colleagues, the Research Associate undertakes theoretical and experimental research
Research Associate (Ecological Remote Sensing)
University of Technology Sydney · Posted 10 days ago
About the role
sciences technologies. We are seeking to engage a Research Associate (Ecological Remote Sensing) for a period of up to 2...'s most liveable cities. With a culturally diverse campus life and extensive international exchange and research programs, UTS prepares
Senior Clinical Research Associate, Neuroscience Trials Australia (NTA)
· Posted 11 days ago
About the role
Are you an experienced Clinical Research Associate ready to take ownership of complex clinical trials and play a key role in advancing..., is seeking a Senior Clinical Research Associate to join our Clinical Operations team. This is an opportunity to work
Research Associate
University of New South Wales · Posted today
About the role
The Opportunity The UNSW Water Research Centre (WRC) has an opportunity for a Research Associate to contribute to research across wastewater management, waste utilisation, hydrogen energy, electrochemistry and materials science. In this role, you will undertake research independently and as part of a collaborative team, contributing to projects focused on developing sustainable solutions across environmental and energy applications. You will apply appropriate research methods to investigate and evaluate new approaches in areas such as resource recovery, waste valorisation, electrochemical systems and advanced materials, while contributing to high-quality research outcomes and the broader development of research activities within the Centre. This position will provide you with the opportunity to further develop your research expertise while contributing to high-quality research outcomes. You will work independently and collaboratively, contribute to scholarly publications and research activities, engage with relevant stakeholders and research partners, participate in conferences and workshops, and assist with the supervision of research students where required. This role reports to Professor Bruce and has no direct reports. Salary, Level A: AUD $118,467 to $126,711 per annum 17% superannuation Employment type: Full time Appointment type: Fixed-term contract – 12-months Location: Kensington – Sydney, Australia About UNSW At UNSW, research is driven by a commitment to creating meaningful impact. Our diverse and talented research community works across disciplines to tackle real-world challenges and advance knowledge. If you want to develop your research career, collaborate with leading researchers and contribute to research that makes a difference, you’re in the right place. The UNSW Water Research Centre (WRC), within the School of Civil and Environmental Engineering, undertakes multidisciplinary research in water and environmental engineering. The Centre works closely with industry, government and research partners to develop innovative solutions to water and environmental challenges. For further information, please go to UNSW Water Research Centre . Skills & Experience A PhD in a related discipline, and/or relevant work experience. Proven commitment to proactively keeping up to date with discipline knowledge and developments. Demonstrated ability to undertake high quality academic research and conduct independent research with limited supervision. Demonstrated track record of publications and conference presentations relative to opportunity. Demonstrated ability to work in a team, collaborate across disciplines and build effective relationships. Evidence of highly developed interpersonal skills. Demonstrated ability to communicate and interact with a diverse range of stakeholders and students. An understanding of and commitment to UNSW’s aims, objectives and values in action, together with relevant policies and guidelines. Knowledge of health and safety responsibilities and commitment to attending relevant health and safety training. Additional details about the specific responsibilities for these positions can be found in the position description. This is available via JOBS@UNSW. To Apply: Please click the “Apply Now” button and submit your CV, Cover Letter and Responses to the Skills and Experience. You should systematically address the Skills and Experience listed within the position description in your application. Please note applications will not be accepted if sent to the contact listed below. Contact: For role-specific inquiries, please contact Professor Bruce Ni E: [email protected] For questions regarding the recruitment process, please contact Eugene Aves (Talent Acquisition Partner) E: [email protected] Applications close: 11:55 pm (Sydney time) on Sunday, 11 October 2026 As part of our recruitment process candidates may be required to undergo pre-employment screening, which may include reference checks, qualification verification, right-to-work verification, and criminal history screening where relevant to the role. UNSW is committed to evolving a culture that embraces equity and supports a diverse and inclusive community where everyone can participate fairly, in a safe and respectful environment. We welcome candidates from all backgrounds and encourage applications from people of diverse gender, sexual orientation, cultural and linguistic backgrounds, Aboriginal and Torres Strait Islander background, people with disability and those with caring and family responsibilities. UNSW provides workplace adjustments for people with disability, and access to flexible work options for eligible staff. The University reserves the right not to proceed with any appointment. LI-DNI
Clinical Research Associate II
ICON · Posted today
About the role
Clinical Research Associate, Home-based in Australia ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers, patients and suppliers. CRA II Home-based in Australia We are currently seeking a Clinical Research Associates to join our diverse and dynamic team. As a Clinical Research Associate at ICON, you will play a pivotal role in designing and analyzing clinical trials, interpreting complex medical data, and contributing to the advancement of innovative treatments and therapies. What you will be doing Conducting site qualification, initiation, monitoring, and close-out visits for clinical trials. Ensuring protocol compliance, data integrity, and patient safety throughout the trial process. Collaborating with investigators and site staff to facilitate smooth study conduct. Performing data review and resolution of queries to maintain high-quality clinical data. Contributing to the preparation and review of study documentation, including protocols and clinical study reports Your profile Bachelor's degree in a scientific or healthcare-related field. Minimum of 2 years of independent monitoring experience as a Clinical Research Associate within CRO/Pharma. In-depth knowledge of clinical trial processes, regulations, and ICH-GCP guidelines. Strong organizational and communication skills, with attention to detail. Ability to work independently and collaboratively in a fast-paced environment. Ability to travel locally and interstate and should possess a valid driver’s license LI-JS1 LI-Remote Employment with ICON is contingent upon having the legal right to work in the country where the role is based. Rewards & Benefits ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development. Benefits may include: Competitive base salary and performance related incentives Health and wellbeing programmes including medical, dental, and vision coverage where applicable Retirement and pension plans Life assurance and disability coverage Employee assistance programmes and wellbeing resources Learning and development opportunities through structured training and career pathways Benefits may vary depending on role and location. Visit our careers site to read more about the benefits ICON offers. Inclusion and Accessibility ICON is an equal opportunity employer. We are committed to building an inclusive and accessible workplace where everyone feels valued and supported. If you require reasonable accommodations during the recruitment process, please let us know or submit a request here . Are you a current ICON Employee? Please click here to apply
Postdoctoral Research Associate in Immunotherapy
University of Sydney · Posted today
About the role
Full time, fixed term until December 2029 Exciting opportunity to be a Postdoctoral Research Associate with Professor Cameron Turtle Base Salary starting from $117,936 17% superannuation About the opportunity We are seeking a Postdoctoral Research Associate in Immunotherapy to contribute to the School’s research agenda through independent and collaborative research. You will apply and develop your research expertise to advance knowledge within your discipline, conduct original research and scholarly activities, and further develop your research profile while working under broad supervision. This role offers the opportunity to collaborate with academic colleagues and research partners, provide informal mentoring and advice to students, and contribute to the broader academic activities and strategic priorities of the School and Faculty. Your key responsibilities will be to: conduct research and scholarly or professional activities independently or as part of a team, contributing to knowledge and advancement within your discipline develop and refine independent research skills under the guidance of more senior academic staff provide informal mentoring and advice to students within your discipline undertake administrative tasks and contribute to Faculty and School meetings contribute to a positive workplace culture that values diversity of thought, collaboration, excellence and outcomes support and contribute to the University’s and Faculty’s strategic priorities undertake other duties and projects appropriate to the classification of the role. About you doctorate or PhD in a relevant field expertise in T cell immunology and analyses of transcription factors in CAR T cells would be an advantage demonstrated understanding of the relevant subject matter and experience conducting original research and/or scholarly activities a developing research profile within your discipline or area of expertise experience developing networks with academic, industry and professional partners or stakeholders strong research, planning and organisational skills effective written and verbal communication skills, including the ability to deliver presentations computer literacy and the ability to work collaboratively with colleagues and stakeholders. Sponsorship / work rights for Australia Work Rights: you must have unrestricted work rights in Australia for the duration of this employment to apply. Visa sponsorship is not available for this appointment. Pre-employment checks Your employment is conditional upon the successful completion of all pre-employment or background checks required for the role in terms satisfactory to the University. Also, to meet the University’s obligations under the National Higher Education Code to Prevent and Eliminate Gender-Based Violence you will be asked to declare if you have been investigated for, or found to engaged in, sexual harm or gender-based violence in the course of previous employment or in a legal process. Similarly, your ongoing employment is conditional upon the satisfactory maintenance of all relevant clearances and background check requirements. If you do not meet these conditions, the University may take any necessary step, including the termination of your employment. EEO statement At the University of Sydney, our shared values are trust, accountability and excellence and we strive to be a place where everyone can thrive. We are committed to creating a University community that thrives through diversity and reflects the wider community that we serve. We deliver on this through our commitment to diversity and inclusion , evidenced by our people and culture programs, as well as key strategies to increase participation and support the careers of Aboriginal and Torres Strait Islander People , women , people living with a disability , people from culturally and linguistically diverse backgrounds , and those who identify as LGBTIQ . We welcome applications from candidates from all backgrounds. We are proud to be recognised as an Australian Workplace Equality Index (AWEI) Gold employer. Find out more about our work on diversity and inclusion . How to apply Applications (including a cover letter, CV, and any additional supporting documentation) can be submitted via the Apply button at the top of the page. For employees of the University or contingent workers, please login into your Workday account and navigate to the Career icon on your Dashboard. Click on USYD Find Jobs and apply. For a confidential discussion about the role, or if you require reasonable adjustment or any documents in alternate formats, please contact, Ajaypal Singh, Recruitment Operations by email to [email protected]. © The University of Sydney The University reserves the right not to proceed with any appointment. Click to view the Position Description for this role. Applications Close Wednesday 11 November 2026 11:59 PM
Senior Clinical Research Associate - NSW
Novotech · Posted today
About the role
Description The Clinical Research Associate (CRA), is primarily responsible for ensuring the rights and wellbeing of trial participants are protected and the reported trial data are accurate, complete, and verifiable from the source documents. The CRA is the primary contact between the Investigational Sites, Novotech and Sponsor. Key responsibility of a CRA is as a site relationship manager ensuring that clinical trials are conducted in accordance with ICH GCP guidelines, local and global regulatory requirements, and Novotech/Client SOPs. This role will be based in Sydney and we offer hybrid working arrangements and full flexibility in working hours to ensure our staff achieve the work-life balance often missing in this role. Minimum Qualifications & Experience Graduate in a clinical or life sciences-related field. Relevant experience/qualifications in allied professions may also be considered. Must have good time management skills, attention to detail, be able to work well in a team, and be computer literate. For our current opportunities we require experience of working in the research, pharmaceutical industry or a related field per job level as follows: SCRA: minimum of 3 years of CRA independent monitoring experience, preferably within Oncology You must have full unrestricted working rights in Australia to be considered for this role . We unfortunately cannot provide sponsorship for this role. Responsibilities: CRAs primary responsibility is to build relationships with Principal Investigators, study coordinators, pharmacists, and all relevant site trial personnel to ensure the efficient, expedited and smooth management of clinical trials. Foster internal and external customer relationships to ensure focus on efficient, timely and productive project delivery as per study requirements and timelines. collaboration with the In-house Clinical Research Associate (IHCRA) and Regulatory Start Up Associate (RSA), prepare site essential documents, and support the ethics and regulatory submission and approval processes as needed. In collaboration with Regulatory Start-up (RSU) Team, understand the requirements of applicable local and international regulatory requirements as relevant to specific clinical trials. Ensure recruitment of participants as per the site target. Drive site recruitment and engagement initiatives and prepare site-specific recruitment plan(s) and update as required. Monitoring of investigational sites as per ICH GCP This includes all monitoring visit types across all phases of a clinical trial including Site Selection, Site Initiation, Site Monitoring and Site Close Out, unblinded pharmacy visits, and co-monitoring visits.
Inhouse Clinical Research Associate - Australia
Novotech · Posted today
About the role
Description The Inhouse Clinical Research Associate (IHCRA) provides in-house support to the clinical team according to project requirements, ICH GCP guidelines, local or global regulatory requirements and Novotech or Client SOPs. Responsibilities Support the clinical team’s inhouse activities on assigned projects. Co-ordinate and maintain clinical study documentation in the Trial Master Files (TMF) including the tracking of documents, preparation for internal/external audits, conducting routine QC reviews and final reconciliation, according to the requirements of ICH GCP and Novotech (or client) SOPs. Support the clinical team in essential document development, collection and management process including any translations according to Good Documentation Practice, ICH GCP and Novotech (or client) SOPs. Manage the Clinical Trial Management System (CTMS), ensuring site compliance scores are maintained to a high level and entered in accordance with company requirements. Follow up with relevant team to update and maintain site milestones, subject tracking and PISCF’s, ensuring accuracy and completeness of the data. Create the Investigator Site Files, co-ordinating the ordering, dispatch and tracking of trial materials (e.g., patient cards and diaries, lab supplies, drug supplies, etc.) according to the logistical requirements of the study. Ensure safe and orderly storage of study materials at Novotech and maintain stock reports as requested by the PM/CRA. May assist the CRAs with the preparation of onsite or remote monitoring visits and follow-up action items from previous monitoring visits. May assist IRB submission (safety reporting: other site SUSAR, Line listing, DSUR, including site communication, CSR submission etc.) including tracker management during project maintenance and close out phase. Minimum Qualifications & Experience: Relevant experience/qualifications in Life Sciences or related field or administration would be preferable. Experience working in the pharmaceutical, CRO or healthcare industry is advantageous. A minimum of 1 years experience as inhouse CRA or relevant clinical administration roles.
Contract Clinical Research Associate
Linical · Posted 1 days ago
About the role
Contract Clinical Research Associate 0.4 FTE Melbourne, Australia Join a global clinical research organization dedicated to advancing innovative therapies and improving patient outcomes. We are seeking an experienced Contract Clinical Research Associate (CRA) to support the successful delivery of clinical trials across Australia. This is a remote, part-time opportunity (0.4 FTE) offering flexibility while working closely with investigative sites and cross-functional study teams. Key Responsibilities Conduct site qualification, initiation, monitoring, and close-out visits. Assess and identify suitable investigative sites and support site selection activities. Train site personnel on study protocols, regulatory requirements, and study procedures. Ensure sites remain compliant with GCP, local regulations, sponsor requirements, and study protocols. Perform source data verification and review clinical documentation for accuracy, completeness, and consistency. Monitor investigational product accountability, storage, dispensing, and reconciliation. Support submissions to Ethics Committees and Regulatory Authorities, as required. Manage site communications, action items, and issue resolution throughout the study lifecycle. Review and maintain essential study documentation within the Trial Master File (TMF). Facilitate data query resolution and ensure timely reporting of study activities. Build and maintain strong relationships with investigators, study coordinators, and internal stakeholders. Participate in study team meetings and contribute to project success. Skills & Qualifications Strong knowledge of clinical trial processes, ICH-GCP guidelines, and applicable regulatory requirements. Excellent written and verbal communication skills. Strong organisational, time management, and problem-solving abilities. Ability to effectively manage multiple priorities and deadlines. Proficient in clinical trial systems and Microsoft Office applications. Strong interpersonal skills and the ability to work collaboratively within global teams. Commitment to quality, accuracy, and patient safety. Ability to travel up to 75% as required. Valid driver's licence. Experience & Education Bachelor's degree in Life Sciences, Nursing, or a related field, or an equivalent combination of education and relevant experience. Successful completion of a recognised CRA training programme. Minimum of 3 years' clinical research experience, including experience as a Clinical Trial Associate, Study Coordinator, Clinical Research Associate, or similar role. Oncology therapeutic experience is preferred. Experience independently conducting site monitoring visits across all phases of a clinical trial. Strong understanding of site management, protocol compliance, patient safety, and data quality requirements.
Senior Clinical Research Associate
IRE · Posted 1 days ago
About the role
Senior Clinical Research Associate - Phase I, Onc- NSW/VIC At ICON Strategic Solutions, you will work in a sponsor-dedicated model, supported by ICON’s global expertise. As the world’s largest FSP organisation, with over 90 sponsor partnerships, we offer stability, career development and a collaborative environment where your work contributes to the development of treatments that benefit patients worldwide. As a Senior CRA at ICON Plc, you will oversee and manage clinical trial activities to ensure they are conducted according to protocol, regulatory requirements, and industry standards. What You Will Do: You will lead on clinical trial monitoring tasks requiring technical depth, with a focus on quality and continuous improvement. Key responsibilities include: Monitoring clinical trial sites to ensure adherence to study protocols, regulatory requirements, and Good Clinical Practice (GCP) standards. Conducting site visits to assess site performance, resolve issues, and provide support to ensure successful trial execution. Collaborating with cross-functional teams to ensure timely and accurate data collection and reporting. Providing training and guidance to site staff and other CRAs to maintain high standards of clinical trial conduct. Building and maintaining effective relationships with site personnel and stakeholders to facilitate smooth trial operations. Your Profile: You will have a strong foundation in clinical trial monitoring, with the experience to work independently and guide others. Required qualifications and experience: Bachelor's degree in a relevant scientific discipline or healthcare-related field Extensive experience as a Clinical Research Associate, with a strong understanding of clinical trial processes and regulatory requirements. Proven ability to manage multiple sites and projects simultaneously, with strong organizational and problem-solving skills. Expertise in monitoring practices, data integrity, and site management, with proficiency in relevant clinical trial software and tools. Excellent communication, interpersonal, and stakeholder management skills, with the ability to influence and drive compliance within a complex environment. Willingness to travel as required (approximately 60%) Employment with ICON is contingent upon having the legal right to work in the country where the role is based. Rewards & Benefits ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development. Benefits may include: Competitive base salary and performance related incentives Health and wellbeing programmes including medical, dental, and vision coverage where applicable Retirement and pension plans Life assurance and disability coverage Employee assistance programmes and wellbeing resources Learning and development opportunities through structured training and career pathways Benefits may vary depending on role and location. Visit our careers site to read more about the benefits ICON offers. Inclusion and Accessibility ICON is an equal opportunity employer. We are committed to building an inclusive and accessible workplace where everyone feels valued and supported. If you require reasonable accommodations during the recruitment process, please let us know or submit a request here . Are you a current ICON Employee? Please click here to apply
Senior Clinical Research Associate
ICON Clinical Research · Posted 1 days ago
About the role
Senior Clinical Research Associate - Phase I, Onc- NSW/VIC At ICON Strategic Solutions, you will work in a sponsor-dedicated model, supported by ICON's global expertise. As the world's largest FSP organisation, with over 90 sponsor partnerships, we offer stability, career development and a collaborative environment where your work contributes to the development of treatments that benefit patients worldwide. As a Senior CRA at ICON Plc, you will oversee and manage clinical trial activities to ensure they are conducted according to protocol, regulatory requirements, and industry standards. What You Will Do: You will lead on clinical trial monitoring tasks requiring technical depth, with a focus on quality and continuous improvement. Key responsibilities include: Monitoring clinical trial sites to ensure adherence to study protocols, regulatory requirements, and Good Clinical Practice (GCP) standards. Conducting site visits to assess site performance, resolve issues, and provide support to ensure successful trial execution. Collaborating with cross-functional teams to ensure timely and accurate data collection and reporting. Providing training and guidance to site staff and other CRAs to maintain high standards of clinical trial conduct. Building and maintaining effective relationships with site personnel and stakeholders to facilitate smooth trial operations. Your Profile: You will have a strong foundation in clinical trial monitoring, with the experience to work independently and guide others. Required qualifications and experience: Bachelor's degree in a relevant scientific discipline or healthcare-related field Extensive experience as a Clinical Research Associate, with a strong understanding of clinical trial processes and regulatory requirements. Proven ability to manage multiple sites and projects simultaneously, with strong organizational and problem-solving skills. Expertise in monitoring practices, data integrity, and site management, with proficiency in relevant clinical trial software and tools. Excellent communication, interpersonal, and stakeholder management skills, with the ability to influence and drive compliance within a complex environment. Willingness to travel as required (approximately 60%) What ICON can offer you: Our success depends on the quality of our people. That's why we've made it a priority to build a diverse culture that rewards high performance and nurtures talent. In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family. Our benefits examples include: Various annual leave entitlements A range of health insurance offerings to suit you and your family's needs. Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead. Global Employee Assistance Programme, LifeWorks, offering 24-hour access to a global network of over 80,000 independent specialized professionals who are there to support you and your family's well-being. Life assurance Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, among others. Visit our careers site (https://careers.iconplc.com/benefits) to read more about the benefits ICON offers. At ICON, inclusion & belonging are fundamental to our culture and values. We're dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know or submit a request here (https://careers.iconplc.com/reasonable-accommodations) Interested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless - there's every chance you're exactly what we're looking for here at ICON whether it is for this or other roles. Are you a current ICON Employee? Please click here (https://wd3.myworkday.com/icon/d/task/1422$1235.htmld) to apply
Research Associate - Chemistry
University of New South Wales · Posted 3 days ago
About the role
One of Australia’s leading research & teaching universities Vibrant campus life with a strong sense of community & inclusion Enjoy a career that makes a difference by collaborating & learning from the best At UNSW, we pride ourselves on being a workplace where the best people come to do their best work. THIS ROLE IS LOCATED IN SYDNEY, AUSTRALIA. The School of Chemistry teaches more than 2000 undergraduate students each year from many different faculties and offers four different undergraduate programs leading to majors in chemistry that are taught in five teaching laboratories specialising in First Year, Synthetic, Analytical and Physical Chemistry. The Research Associate contributes to research on electrochemical aptamer based sensors as part of an ARC funded Laureate project. This role performs fundamental electrochemical research on developing electrodes that can provide insights into developing these sensors and how they can be transitioned to commercialisation. About the role $118K - $126K plus 17% Superannuation and annual leave loading Fixed Term – 12 months Full-time (35 hours per week) The role of Research Associate reports to Scientia Professor Justin Gooding and has no direct reports. Specific responsibilities for this role include: Conduct research in the area of electrochemistry and biosensors. Perform and supervise experiments in electrochemical aptamer-based sensors. Write and maintain laboratory notebooks detailing all experiments conducted. Successfully complete experiments and on-time provision of analysis on results. Analyse and write results of experiments in a format suitable for publication in peer reviewed journals. Contribute to the writing of scientific papers and reports for international journals and progress reporting to other researchers and industry partners. Contribute to the preparation of research proposal submissions to funding bodies and actively seek collaboration with industry partners as appropriate. Assist with the coordination of research activities and actively contribute to research outputs to meet project milestones. Present results of experiments at national and international conferences. Assist in the training of PhD and honours students. Align with and actively demonstrate the Code of Conduct and Values. Cooperate with all health and safety policies and procedures of the university and take all reasonable care to ensure that your actions or omissions do not impact on the psychosocial or physical health and safety of yourself or others. About the successful applicant (Selection Criteria) To be successful in this role you will have: A PhD specialising in electrochemistry. Demonstrated ability to develop electrochemical procedures for surface characterisation. Extensive experience in performing electrochemical measurements. Demonstrated experience in materials synthesis. Previous experience in a research environment and in training PhD and Honours Students. Demonstrated ability to undertake high quality academic research and conduct independent research with limited supervision. Demonstrated track record of publications and conference presentations relative to opportunity. Demonstrated ability to work in a team, collaborate across disciplines and build effective relationships. Evidence of highly developed interpersonal skills. Demonstrated ability to communicate and interact with a diverse range of stakeholders and students. An understanding of and commitment to UNSW’s aims, objectives and values in action, together with relevant policies and guidelines. Knowledge of health and safety responsibilities and commitment to attending relevant health and safety training. You should systematically address the selection criteria listed above in your application. Please apply online - applications will not be accepted if sent to the contact listed. Contact: Justin Gooding E: [email protected] Applications close: November 9th, 2026 Find out more about working at UNSW at www.unsw.edu.au UNSW is committed to equity diversity and inclusion. Applications from women, people of culturally and linguistically diverse backgrounds, those living with disabilities, members of the LGBTIQ community; and people of Aboriginal and Torres Strait Islander descent, are encouraged. UNSW provides workplace adjustments for people with disability, and access to flexible work options for eligible staff. The University reserves the right not to proceed with any appointment.
Senior Clinical Research Associate
PSI CRO · Posted 4 days ago
About the role
Company Description We are the company that cares – for our staff, for our clients, for our partners and for the quality of the work we do. A dynamic, global company founded in 1995, we bring together 3000 driven, dedicated and passionate individuals. We work on the frontline of medical science, changing lives, and bringing new medicines to those who need them. PSI’s business is about conducting clinical research of novel medications. We work at the interface of R&D, pharmaceutical industry and healthcare science and provide services to big and mid-sized pharmaceutical companies. We help our clients to generate data about safety and efficacy of medications and bring the best ones to market. By conducting global clinical research trials, PSI makes cutting-edge treatment available in drugstores all over the world and helps patients with serious medical conditions to improve or even save their life. Help us to make sure that PSI medical and business documents are clear to patients, physicians, regulatory authorities, and clients. We offer an inspiring story of the company that has grown organically from a handful of countries to global presence. PSI is a mature company with standards and practices, but we do not stand still. Every day, there is a figurative Everest to climb, and you will not get bored here. Job Description We’re searching for a knowledgeable, team-oriented Senior CRA to manage the clinical aspects of full-service global projects in Australia. As a Senior CRA at PSI, you will work on the frontline of communication with project stakeholders, ensuring timelines, targets and standards of clinical research projects in a variety of therapeutic indications. You will build and maintain relationships with clinical sites and investigators. You will focus on subjects’ rights, safety and well-being and quality of data compliance. Training, mentoring and supervising study level responsibilities for Jr. CRAs Preparation, conduct, and reporting of selection, initiation, routine and closeout monitoring visits Delivering training of investigators, site staff and project teams Work with complex studies Perform CRF review, source document verification and query resolution Be responsible for site communication and management Be involved in site identification process Contact for clinical investigators, vendors and support services in regard to study progress Participate in feasibility research Preparation and delivering of presentations at Investigator’s Meetings Preparation for and attendance at company’s audits; resolution of audit findings Support to Regulatory Affairs in procurement of site regulatory documents Maintenance of study-specific automated tracking systems Qualifications College/University degree in Life Sciences or an equivalent combination of education, training & experience At least 4 years of independent on-site monitoring experience in Australia Experience in all types of monitoring visits in Phase II and/or III Availability to travel Experience in Inflammatory Bowel Disease, Oncology, Infectious Diseases is a plus Proficiency in MS Office applications Ability to plan and work in a dynamic team environment Communication, collaboration, and problem-solving skills If you like to train and support others on their clinical research steps, and are also looking forward to future Lead Monitor roles, this position may just be the right one for you. Additional Information What you’ll get: Competitive salary We offer hybrid work arrangement - 2 days flexi and 3 days in office (Sydney-based only) Access to a wide range of employee benefits such as onsite Gym access (Sydney-based only) Additional 5 days of wellness leave Development and learning opportunities Chance to make a real impact in a meaningful industry PSI is a passionate, organically grown, and award-winning full-service CRO who dares to be different. As a dynamic and global company, we bring together more than 3000 driven and dedicated experts across 60 countries working collectively to help make a positive impact on patient lives. How are we different? PSI is privately owned by the very people who founded the company 30 years ago, and they’re still working here today. As a result, we have grown organically around the globe and have kept our company fully independent, giving us significant advantages and freedoms. Being a Part of the Team As a part of the PSI team, you will have a fair degree of ownership and autonomy to make nuanced country-and department-specific adjustments while nurturing the global PSI culture that unites us across six continents. You will receive continuous support from your global peers and join a fast-paced, innovative, and results-oriented working environment with lean communication lines. We pride ourselves on being approachable, receptive to new ideas, and open to feedback. Growth Opportunities PSI is proud to invest in our people, from entry-level team members to senior leaders, helping you identify and hone your unique strengths at every step of your career. From on-the-job learning experiences to formal development programs, our professionals have a variety of opportunities to continue to grow throughout their career.
Clinical Research Associate 3
ICON Clinical Research · Posted 5 days ago
About the role
CRA III Adelaide, Australia - Remote At ICON Strategic Solutions, you will work in a sponsor-dedicated model, supported by ICON's global expertise. As the world's largest FSP organisation, with over 90 sponsor partnerships, we offer stability, career development and a collaborative environment where your work contributes to the development of treatments that benefit patients worldwide. As a Senior CRA at ICON Plc, you will oversee and manage clinical trial activities to ensure they are conducted according to protocol, regulatory requirements, and industry standards. What You Will Do: You will lead on clinical trial monitoring tasks requiring technical depth, with a focus on quality and continuous improvement. Key responsibilities include: Monitoring clinical trial sites to ensure adherence to study protocols, regulatory requirements, and Good Clinical Practice (GCP) standards. Conducting site visits to assess site performance, resolve issues, and provide support to ensure successful trial execution. Collaborating with cross-functional teams to ensure timely and accurate data collection and reporting. Providing training and guidance to site staff and other CRAs to maintain high standards of clinical trial conduct. Building and maintaining effective relationships with site personnel and stakeholders to facilitate smooth trial operations. Your Profile: You will have a strong foundation in clinical trial monitoring, with the experience to work independently and guide others. Required qualifications and experience: Bachelor's degree in a relevant scientific discipline or healthcare-related field Extensive experience as a Clinical Research Associate, with a strong understanding of clinical trial processes and regulatory requirements. Proven ability to manage multiple sites and projects simultaneously, with strong organizational and problem-solving skills. Expertise in monitoring practices, data integrity, and site management, with proficiency in relevant clinical trial software and tools. Excellent communication, interpersonal, and stakeholder management skills, with the ability to influence and drive compliance within a complex environment. Willingness to travel as required (approximately 60%) What ICON can offer you: Our success depends on the quality of our people. That's why we've made it a priority to build a diverse culture that rewards high performance and nurtures talent. In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family. Our benefits examples include: Various annual leave entitlements A range of health insurance offerings to suit you and your family's needs. Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead. Global Employee Assistance Programme, LifeWorks, offering 24-hour access to a global network of over 80,000 independent specialized professionals who are there to support you and your family's well-being. Life assurance Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, among others. Visit our careers site (https://careers.iconplc.com/benefits) to read more about the benefits ICON offers. At ICON, inclusion & belonging are fundamental to our culture and values. We're dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know or submit a request here (https://careers.iconplc.com/reasonable-accommodations) Interested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless - there's every chance you're exactly what we're looking for here at ICON whether it is for this or other roles. Are you a current ICON Employee? Please click here (https://wd3.myworkday.com/icon/d/task/1422$1235.htmld) to apply
Experienced Clinical Research Associate
Jobgether · Posted 6 days ago
About the role
This position is listed on behalf of a partner company, which manages all applications and next steps. Our partner is looking for an Experienced Clinical Research Associate based in Australia. Join a dynamic clinical research environment dedicated to advancing the development of safe and effective medical treatments. In this home-based role, you will oversee clinical trial activities across multiple research sites, ensuring data integrity, regulatory compliance, and adherence to study protocols. You will collaborate closely with investigators, physicians, research coordinators, and site teams to maintain high standards of clinical research quality. Your expertise will help protect participant safety, improve trial performance, and support the delivery of reliable clinical data. With structured training, flexible working arrangements, and performance-based incentives, this opportunity offers both professional autonomy and meaningful career development. You will also have opportunities to grow into leadership roles and contribute to clinical research that makes a difference to patients worldwide. Accountabilities: Conduct site qualification, initiation, monitoring, and closeout visits in accordance with approved study protocols, Good Clinical Practice (GCP), standard operating procedures (SOPs), and applicable regulatory requirements. Build and maintain effective working relationships with clinical investigators, research physicians, study coordinators, and other site personnel. Assess investigator qualifications, training, staffing, facilities, laboratories, equipment, and other resources to ensure sites are adequately prepared to conduct clinical trials. Verify clinical data against medical records and source documentation, ensuring accuracy, completeness, consistency, and compliance with good documentation practices. Identify data entry errors, protocol deviations, and compliance issues, communicate findings to site teams, and recommend appropriate corrective actions. Confirm that participant recruitment and enrollment comply with study eligibility criteria, and assess site recruitment and retention performance while recommending improvements where needed. Review regulatory documentation and oversee investigational product accountability, inventory management, and related records. Verify the accurate reporting of adverse events, serious adverse events, concomitant medications, and relevant medical conditions in accordance with study protocols and reporting requirements. Prepare comprehensive monitoring reports and follow-up letters, documenting significant findings, deviations, deficiencies, and recommended actions to maintain site compliance and data quality. Requirements: Bachelor's degree in a health-related or scientific discipline. At least 1.5 to 5 years of experience in clinical monitoring, preferably with demonstrated experience conducting clinical trial site visits and managing monitoring activities. Solid knowledge of clinical monitoring practices, clinical trial processes, GCP principles, regulatory requirements, and applicable SOPs. Ability to assess site performance, review clinical and regulatory documentation, identify compliance risks, and communicate findings effectively. Strong interpersonal, organizational, analytical, and problem-solving skills, with the ability to collaborate with multidisciplinary teams and manage competing priorities. Excellent written and verbal communication skills, including the ability to prepare clear monitoring reports and follow-up documentation. Confidence representing clinical monitoring expertise in internal and external meetings, including discussions with business development teams when required. Ability to work independently in a home-based environment while maintaining effective communication with study teams and research sites. Candidates based in Sydney, Brisbane, Adelaide, or Perth are preferred. Visa sponsorship or transfer may be available for qualified candidates already based in Australia. Benefits: Flexible, home-based working arrangements and flexible working hours. No minimum monthly requirement for days spent on-site. Competitive compensation package and transportation allowance. Performance-based variable compensation, with bonuses calculated directly according to the number of monitoring visits completed. Annual merit-based salary increases. Accelerated, personalized training tailored to your existing experience. Opportunities to progress into senior and leadership positions, including Lead CRA, CRA Manager, and Clinical Trial Manager roles. Airline club allowance. Casual dress code. Opportunities for continuous professional development, cross-functional collaboration, and long-term career growth. A collaborative, science-driven environment focused on clinical research quality, innovation, and improving patient outcomes. How Jobgether works: We use an AI-powered matching process to ensure your application is reviewed quickly, objectively, and fairly against the role's core requirements. Our system identifies the top-fitting candidates, and this shortlist is then shared directly with the hiring company. The final decision and next steps (interviews, assessments) are managed by their internal team. We appreciate your interest and wish you the best! Why Apply Through Jobgether? Data Privacy Notice: By submitting your application, you acknowledge that Jobgether will process your personal data to evaluate your candidacy and share relevant information with the hiring employer. This processing is based on legitimate interest and pre-contractual measures under applicable data protection laws (including GDPR). You may exercise your rights (access, rectification, erasure, objection) at any time. LI-CL1 We may use artificial intelligence (AI) tools to support parts of the hiring process, such as reviewing applications, analyzing resumes, or assessing responses and identifying potential inconsistencies or verification signals in application materials based on available information. These tools assist our recruitment team but do not replace human judgment. Final hiring decisions are ultimately made by humans. If you would like more information about how your data is processed, please contact us.
Clinical Research Associate 3
ICON · Posted 7 days ago
About the role
CRA III Adelaide, Australia - Remote At ICON Strategic Solutions, you will work in a sponsor-dedicated model, supported by ICON’s global expertise. As the world’s largest FSP organisation, with over 90 sponsor partnerships, we offer stability, career development and a collaborative environment where your work contributes to the development of treatments that benefit patients worldwide. As a Senior CRA at ICON Plc, you will oversee and manage clinical trial activities to ensure they are conducted according to protocol, regulatory requirements, and industry standards. What You Will Do: You will lead on clinical trial monitoring tasks requiring technical depth, with a focus on quality and continuous improvement. Key responsibilities include: Monitoring clinical trial sites to ensure adherence to study protocols, regulatory requirements, and Good Clinical Practice (GCP) standards. Conducting site visits to assess site performance, resolve issues, and provide support to ensure successful trial execution. Collaborating with cross-functional teams to ensure timely and accurate data collection and reporting. Providing training and guidance to site staff and other CRAs to maintain high standards of clinical trial conduct. Building and maintaining effective relationships with site personnel and stakeholders to facilitate smooth trial operations. Your Profile: You will have a strong foundation in clinical trial monitoring, with the experience to work independently and guide others. Required qualifications and experience: Bachelor's degree in a relevant scientific discipline or healthcare-related field Extensive experience as a Clinical Research Associate, with a strong understanding of clinical trial processes and regulatory requirements. Proven ability to manage multiple sites and projects simultaneously, with strong organizational and problem-solving skills. Expertise in monitoring practices, data integrity, and site management, with proficiency in relevant clinical trial software and tools. Excellent communication, interpersonal, and stakeholder management skills, with the ability to influence and drive compliance within a complex environment. Willingness to travel as required (approximately 60%) Employment with ICON is contingent upon having the legal right to work in the country where the role is based. Rewards & Benefits ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development. Benefits may include: Competitive base salary and performance related incentives Health and wellbeing programmes including medical, dental, and vision coverage where applicable Retirement and pension plans Life assurance and disability coverage Employee assistance programmes and wellbeing resources Learning and development opportunities through structured training and career pathways Benefits may vary depending on role and location. Visit our careers site to read more about the benefits ICON offers. Inclusion and Accessibility ICON is an equal opportunity employer. We are committed to building an inclusive and accessible workplace where everyone feels valued and supported. If you require reasonable accommodations during the recruitment process, please let us know or submit a request here . Are you a current ICON Employee? Please click here to apply
Senior Clinical Research Associate
PSI CRO · Posted 8 days ago
About the role
Job Description We’re searching for a knowledgeable, team-oriented Senior CRA to manage the clinical aspects of full-service global projects in Australia. As a Senior CRA at PSI, you will work on the frontline of communication with project stakeholders, ensuring timelines, targets and standards of clinical research projects in a variety of therapeutic indications. You will build and maintain relationships with clinical sites and investigators. You will focus on subjects’ rights, safety and well-being and quality of data compliance. Location: Macquarie Park, NSW Training, mentoring and supervising study level responsibilities for Jr. CRAs Preparation, conduct, and reporting of selection, initiation, routine and closeout monitoring visits Delivering training of investigators, site staff and project teams Work with complex studies Perform CRF review, source document verification and query resolution Be responsible for site communication and management Be involved in site identification process Contact for clinical investigators, vendors and support services in regard to study progress Participate in feasibility research Preparation and delivering of presentations at Investigator’s Meetings Preparation for and attendance at company’s audits; resolution of audit findings Support to Regulatory Affairs in procurement of site regulatory documents Maintenance of study-specific automated tracking systems
Clinical Research Associate
IQVIA · Posted 9 days ago
About the role
Are you a Clinical Research Associate looking for your next big adventure? Look no further than IQVIA, a global CRO with outstanding reputation. Our CRA teams have current openings across various locations in Australia. *Visa sponsorship for candidates that meet the requirements and eligibility. Only suitable candidates will be contacted. The role: Perform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study data as required by the study protocol, applicable regulations and guidelines, and sponsor requirements. Essential Functions Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance with contracted scope of work and regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines Work with sites to adapt, drive, and track subject recruitment plan in line with project needs to enhance predictability. Administer protocol and related study training to assigned sites and establish regular lines of communication with sites to manage ongoing project expectations and issues. Evaluate the quality and integrity of study site practices related to the proper conduct of the protocol and adherence to applicable regulations. Escalate quality issues as appropriate. Manage the progress of assigned studies by tracking regulatory submissions and approvals, recruitment and enrollment, case report form (CRF) completion and submission, and data query generation and resolution. May support start-up phase. Ensure copies/originals (as required) site documents are available for filing in the Trial Master File (TMF) and verify that the Investigator's Site File (ISF) is maintained in accordance with GCP and local regulatory requirements. Create and maintain appropriate documentation regarding site management, monitoring visit findings and action plans by submitting regular visit reports, generating follow-up letters and other required study documentation. Collaborate and liaise with study team members for project execution support as appropriate. If applicable, may be accountable for supporting development of project subject recruitment plan on a per site basis. If applicable, may be accountable for site financial management according to executed clinical trial agreement and retrieve invoices according to local requirement. Qualifications Bachelor's Degree in scientific discipline or health care. Requires at least 9 months of independent on-site monitoring experience. Equivalent combination of education, training and experience may be accepted in lieu of degree. Good knowledge of, and skill in applying, applicable clinical research regulatory requirements (i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines). Good therapeutic and protocol knowledge as provided in company training. Computer skills including proficiency in use of Microsoft Word, Excel and PowerPoint and use of a laptop computer and iPhone and iPad (where applicable). Organizational and problem-solving skills. Effective time and financial management skills. Ability to establish and maintain effective working relationships with coworkers, managers, and clients. Candidates will be assessed according to their years of experience and be considered for various levels where applicable. What's in it for you? Flexible hybrid work environment, with an office in the heart of Melbourne and Sydney. Competitive salary with car and health allowances. Career growth and opportunity across our FSO and FSP models. Work with skilled Managers across multi-phases clinical trials If you are interested and meet the skills and experience above, please apply with your resume today. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.
Senior / Clinical Research Associate
IQVIA · Posted 9 days ago
About the role
Are you a Senior/Clinical Research Associate looking for your next big adventure? Look no further than IQVIA, a global CRO with outstanding reputation. Our CRA teams have current openings across various locations in Australia. *Visa sponsorship for candidates that meet the requirements and eligibility. Only suitable candidates will be contacted. The role: Perform monitoring and site management work to ensure that sites are conducting the studies and reporting study data as required by the study protocol, applicable regulations and guidelines, and sponsor requirements. Essential Functions Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance with contracted scope of work and regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines Work with sites to adapt, drive, and track subject recruitment plan in line with project needs to enhance predictability. Administer protocol and related study training to assigned sites and establish regular lines of communication with sites to manage ongoing project expectations and issues. Evaluate the quality and integrity of study site practices related to the proper conduct of the protocol and adherence to applicable regulations. Escalate quality issues as appropriate. Manage the progress of assigned studies by tracking regulatory submissions and approvals, recruitment and enrollment, case report form (CRF) completion and submission, and data query generation and resolution. May support start-up phase. Ensure copies/originals (as required) site documents are available for filing in the Trial Master File (TMF) and verify that the Investigator's Site File (ISF) is maintained in accordance with GCP and local regulatory requirements. Create and maintain appropriate documentation regarding site management, monitoring visit findings and action plans by submitting regular visit reports, generating follow-up letters and other required study documentation. Collaborate and liaise with study team members for project execution support as appropriate. If applicable, may be accountable for supporting development of project subject recruitment plan on a per site basis. If applicable, may be accountable for site financial management according to executed clinical trial agreement and retrieve invoices according to local requirement. Qualifications Bachelor's Degree in scientific discipline or health care. Requires at least 9 months of independent on-site monitoring experience. Equivalent combination of education, training and experience may be accepted in lieu of degree. Good knowledge of, and skill in applying, applicable clinical research regulatory requirements (i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines). Good therapeutic and protocol knowledge as provided in company training. Computer skills including proficiency in use of Microsoft Word, Excel and PowerPoint and use of a laptop computer and iPhone and iPad (where applicable). Organizational and problem-solving skills. Effective time and financial management skills. Ability to establish and maintain effective working relationships with coworkers, managers, and clients. Candidates will be assessed according to their years of experience and be considered for various levels where applicable. What's in it for you? Flexible hybrid work environment, with an office in the heart of Melbourne and Sydney. Competitive salary with car and health allowances. Career growth and opportunity across our FSO and FSP models. Work with skilled Managers across multi-phases clinical trials If you are interested and meet the skills and experience above, please apply with your resume today. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.
Clinical Research Associate II
PSI CRO · Posted 9 days ago
About the role
Company Description We are the company that cares – for our staff, for our clients, for our partners and for the quality of the work we do. A dynamic, global company founded in 1995, we bring together 3000 driven, dedicated and passionate individuals. We work on the frontline of medical science, changing lives, and bringing new medicines to those who need them. PSI’s business is about conducting clinical research of novel medications. We work at the interface of R&D, pharmaceutical industry and healthcare science and provide services to big and mid-sized pharmaceutical companies. We help our clients to generate data about safety and efficacy of medications and bring the best ones to market. By conducting global clinical research trials, PSI makes cutting-edge treatment available in drugstores all over the world and helps patients with serious medical conditions to improve or even save their life. Help us to make sure that PSI medical and business documents are clear to patients, physicians, regulatory authorities, and clients. We offer an inspiring story of the company that has grown organically from a handful of countries to global presence. PSI is a mature company with standards and practices, but we do not stand still. Every day, there is a figurative Everest to climb, and you will not get bored here. Job Description We’re searching for a knowledgeable, team-oriented CRA II to manage the clinical aspects of full-service global projects in Australia. As a CRA II at PSI, you will work on the frontline of communication with project stakeholders, ensuring timelines, targets and standards of clinical research projects in a variety of therapeutic indications. You will build and maintain relationships with clinical sites and investigators. You will focus on subjects’ rights, safety and well-being and quality of data compliance. Location: Macquarie Park, NSW You will: Conduct and report all types of onsite monitoring visits Be involved in study startup Perform CRF review, source document verification and query resolution Facilitate site budgets and contract negotiations Monitor trial progress on the country level Be responsible for site communication and management Be a point of contact for in-house support services and vendors Communicate with internal project teams regarding study progress Participate in feasibility research Support regulatory team in preparing documents for study submissions Qualifications College/University degree in Life Sciences, Pharmacy, RN or an equivalent combination of education, training & experience At least 2 years of independent on-site monitoring experience in Australia Experience in all types of monitoring visits in Phase II and/or III Experience in Inflammatory Bowel Disease, Oncology, Infectious Diseases is a plus Full working proficiency in English PC skills to be able to work with MS Word, Excel and PowerPoint Ability to plan, multitask and work in a dynamic team environment Communication, collaboration, and problem-solving skills Ability to travel Candidate outside of NSW is encouraged to apply! Additional Information What you’ll get: Competitive salary We offer hybrid work arrangement - 2 days flexi and 3 days in office Access to a wide range of employee benefits such as onsite Gym access Additional 5 days of wellness leave Development and learning opportunities Chance to make a real impact in a meaningful industry About Us PSI is a passionate, organically grown, and award-winning full-service CRO who dares to be different. As a dynamic and global company, we bring together more than 3000 driven and dedicated experts across 60 countries working collectively to help make a positive impact on patient lives. How are we different? PSI is privately owned by the very people who founded the company 30 years ago, and they’re still working here today. As a result, we have grown organically around the globe and have kept our company fully independent, giving us significant advantages and freedoms. Being a Part of the Team As a part of the PSI team, you will have a fair degree of ownership and autonomy to make nuanced country-and department-specific adjustments while nurturing the global PSI culture that unites us across six continents. You will receive continuous support from your global peers and join a fast-paced, innovative, and results-oriented working environment with lean communication lines. We pride ourselves on being approachable, receptive to new ideas, and open to feedback. Growth Opportunities PSI is proud to invest in our people, from entry-level team members to senior leaders, helping you identify and hone your unique strengths at every step of your career. From on-the-job learning experiences to formal development programs, our professionals have a variety of opportunities to continue to grow throughout their career.
Clinical Research Associate II
PSI CRO · Posted 10 days ago
About the role
Job Description We’re searching for a knowledgeable, team-oriented CRA II to manage the clinical aspects of full-service global projects in Australia. As a CRA II at PSI, you will work on the frontline of communication with project stakeholders, ensuring timelines, targets and standards of clinical research projects in a variety of therapeutic indications. You will build and maintain relationships with clinical sites and investigators. You will focus on subjects’ rights, safety and well-being and quality of data compliance. Location: Macquarie Park, NSW You will: Conduct and report all types of onsite monitoring visits Be involved in study startup Perform CRF review, source document verification and query resolution Facilitate site budgets and contract negotiations Monitor trial progress on the country level Be responsible for site communication and management Be a point of contact for in-house support services and vendors Communicate with internal project teams regarding study progress Participate in feasibility research Support regulatory team in preparing documents for study submissions
Research Associate
University of Sydney · Posted 13 days ago
About the role
Full time, 12 month fixed term Contribute to the use of AI in medical imaging Base Salary $ 117,936 - $125,896 (Academic level A) 17% superannuation About the opportunity We have an opportunity for a Postdoctoral Research Associate (Level A) in Clinical Imaging to join a successful and supportive research team to work on a research project harnessing the power of artificial-intelligence (AI) to improve radiation therapy treatment for cancer patients. The Postdoctoral Research Associate Clinical Imaging will build and clinically translate new cancer targeting technologies based on Artificial Intelligence and x-ray imaging that solve the challenges of complex patient motion during radiation therapy. Based at South Eveleigh, the Image X Institute’s research portfolio spans development of new treatment ideas, clinical trials, preclinical imaging, device development, radiation therapy physics, and computational physics. We engage with industry, hospitals, international collaborators and universities to forge relationships that help take our projects from lab bench to patient bedside. Enjoy working in a supportive environment with access to unique medical data sets and a chance to make practice changing impacts in real time image guidance for cancer radiotherapy. Your key responsibilities will be to: advance the algorithms of imaging and targeted radiation therapy create, develop and experimentally and clinically implement AI based algorithms support the acquisition and analysis of clinical data, and imaging, software and equipment infrastructure contribute to scientific publications, research dissemination and the development of competitive funding proposals undertake clinical site visits to support technology installation, testing and implementation, as required. About you completion or nearing completion of PhD in physics, computer science, applied mathematics or biomedical engineering or relevant discipline demonstrated track record of publishing research findings in peer-reviewed scientific journals knowledge of software and mathematical algorithm development, especially in artificial intelligence some experience supporting the clinical integration, implementation and translation of research technologies into clinical practice. some experience collaborating with multidisciplinary teams, including radiation oncologists, medical physicists, engineers and other clinical professionals. Sponsorship / work rights for Australia You must have unrestricted work rights in Australia for the duration of this employment to be eligible to apply. Visa sponsorship is not available for this appointment. Pre-employment checks Your employment is conditional upon the completion of all role required pre-employment or background checks in terms satisfactory to the University. Similarly, your ongoing employment is conditional upon the satisfactory maintenance of all relevant clearances and background check requirements. If you do not meet these conditions, the University may take any necessary step, including the termination of your employment. EEO statement At the University of Sydney, our shared values are trust, accountability and excellence and we strive to be a place where everyone can thrive. We are committed to creating a University community that thrives through diversity and reflects the wider community that we serve. We deliver on this through our commitment to diversity and inclusion , evidenced by our people and culture programs, as well as key strategies to increase participation and support the careers of Aboriginal and Torres Strait Islander People , women , people living with a disability , people from culturally and linguistically diverse backgrounds , and those who identify as LGBTQIA . We welcome applications from candidates from all backgrounds. We are proud to be recognised as an Australian Workplace Equality Index (AWEI) Platinum Employer. Find out more about our work on diversity and inclusion . How to apply Applications (including a cover letter, CV, and any additional supporting documentation) can be submitted via the Apply button at the top of the page. For employees of the University or contingent workers, please login into your Workday account and navigate to the Career icon on your Dashboard. Click on USYD Find Jobs and apply. For a confidential discussion about the role, or if you require reasonable adjustment or any documents in alternate formats, please contact Lena Germinarios , Recruitment Operations by email to [email protected] . © The University of Sydney The University reserves the right not to proceed with any appointment. Click to view the Position Description for this role. Applications Close Sunday 01 November 2026 11:59 PM
Clinical Research Associate 3
IRE · Posted 13 days ago
About the role
SCRA - Australia - Remote/Hybrid At ICON Strategic Solutions, you will work in a sponsor-dedicated model, supported by ICON’s global expertise. As the world’s largest FSP organisation, with over 90 sponsor partnerships, we offer stability, career development and a collaborative environment where your work contributes to the development of treatments that benefit patients worldwide. As a Senior CRA at ICON Plc, you will oversee and manage clinical trial activities to ensure they are conducted according to protocol, regulatory requirements, and industry standards. What You Will Do: You will lead on clinical trial monitoring tasks requiring technical depth, with a focus on quality and continuous improvement. Key responsibilities include: Monitoring clinical trial sites to ensure adherence to study protocols, regulatory requirements, and Good Clinical Practice (GCP) standards. Conducting site visits to assess site performance, resolve issues, and provide support to ensure successful trial execution. Collaborating with cross-functional teams to ensure timely and accurate data collection and reporting. Providing training and guidance to site staff and other CRAs to maintain high standards of clinical trial conduct. Building and maintaining effective relationships with site personnel and stakeholders to facilitate smooth trial operations. Your Profile: You will have a strong foundation in clinical trial monitoring, with the experience to work independently and guide others. Required qualifications and experience: Bachelor's degree in a relevant scientific discipline or healthcare-related field Extensive experience as a Clinical Research Associate, with a strong understanding of clinical trial processes and regulatory requirements. Proven ability to manage multiple sites and projects simultaneously, with strong organizational and problem-solving skills. Expertise in monitoring practices, data integrity, and site management, with proficiency in relevant clinical trial software and tools. Excellent communication, interpersonal, and stakeholder management skills, with the ability to influence and drive compliance within a complex environment. Willingness to travel as required (approximately 60%) Employment with ICON is contingent upon having the legal right to work in the country where the role is based. Rewards & Benefits ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development. Benefits may include: Competitive base salary and performance related incentives Health and wellbeing programmes including medical, dental, and vision coverage where applicable Retirement and pension plans Life assurance and disability coverage Employee assistance programmes and wellbeing resources Learning and development opportunities through structured training and career pathways Benefits may vary depending on role and location. Visit our careers site to read more about the benefits ICON offers. Inclusion and Accessibility ICON is an equal opportunity employer. We are committed to building an inclusive and accessible workplace where everyone feels valued and supported. If you require reasonable accommodations during the recruitment process, please let us know or submit a request here . Are you a current ICON Employee? Please click here to apply
Clinical Research Associate 3
ICON Clinical Research · Posted 13 days ago
About the role
SCRA - Australia - Remote/Hybrid At ICON Strategic Solutions, you will work in a sponsor-dedicated model, supported by ICON's global expertise. As the world's largest FSP organisation, with over 90 sponsor partnerships, we offer stability, career development and a collaborative environment where your work contributes to the development of treatments that benefit patients worldwide. As a Senior CRA at ICON Plc, you will oversee and manage clinical trial activities to ensure they are conducted according to protocol, regulatory requirements, and industry standards. What You Will Do: You will lead on clinical trial monitoring tasks requiring technical depth, with a focus on quality and continuous improvement. Key responsibilities include: Monitoring clinical trial sites to ensure adherence to study protocols, regulatory requirements, and Good Clinical Practice (GCP) standards. Conducting site visits to assess site performance, resolve issues, and provide support to ensure successful trial execution. Collaborating with cross-functional teams to ensure timely and accurate data collection and reporting. Providing training and guidance to site staff and other CRAs to maintain high standards of clinical trial conduct. Building and maintaining effective relationships with site personnel and stakeholders to facilitate smooth trial operations. Your Profile: You will have a strong foundation in clinical trial monitoring, with the experience to work independently and guide others. Required qualifications and experience: Bachelor's degree in a relevant scientific discipline or healthcare-related field Extensive experience as a Clinical Research Associate, with a strong understanding of clinical trial processes and regulatory requirements. Proven ability to manage multiple sites and projects simultaneously, with strong organizational and problem-solving skills. Expertise in monitoring practices, data integrity, and site management, with proficiency in relevant clinical trial software and tools. Excellent communication, interpersonal, and stakeholder management skills, with the ability to influence and drive compliance within a complex environment. Willingness to travel as required (approximately 60%) What ICON can offer you: Our success depends on the quality of our people. That's why we've made it a priority to build a diverse culture that rewards high performance and nurtures talent. In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family. Our benefits examples include: Various annual leave entitlements A range of health insurance offerings to suit you and your family's needs. Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead. Global Employee Assistance Programme, LifeWorks, offering 24-hour access to a global network of over 80,000 independent specialized professionals who are there to support you and your family's well-being. Life assurance Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, among others. Visit our careers site (https://careers.iconplc.com/benefits) to read more about the benefits ICON offers. At ICON, inclusion & belonging are fundamental to our culture and values. We're dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know or submit a request here (https://careers.iconplc.com/reasonable-accommodations) Interested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless - there's every chance you're exactly what we're looking for here at ICON whether it is for this or other roles. Are you a current ICON Employee? Please click here (https://wd3.myworkday.com/icon/d/task/1422$1235.htmld) to apply
In-House Clinical Research Associate I
Worldwide Clinical Trials · Posted 13 days ago
About the role
Who we are We’re a global, midsize CRO that pushes boundaries, innovates and invents because the path to a cure for the world’s most persistent diseases is not paved by those who play it safe. It is built by those who take pioneering, creative approaches and implement them with quality and excellence. We are Worldwide Clinical Trials, and we are a global team of over 3,500 experts, bright thinkers, dreamers and doers and, together, we are changing the way the world experiences CROs – in the best possible way. Our mission is to work with passion and purpose every day to improve lives and we are looking for others who value this same pursuit. Why Worldwide We believe everyone plays an important role in making a world of difference for patients and their caregivers. From our hands-on, accessible leaders, to our cohesive and supportive teams, we are committed to enabling professionals from all backgrounds and experiences to succeed. We prioritize cultivating a diverse and inclusive environment that continues to promote collaboration and creativity. We are proud to be a workplace where people thrive by being themselves and are inspired to do their best work every day. Join us! Make an Impact as an Inhouse Clinical Research Associate at Worldwide As an Inhouse Clinical Research Associate, you'll play an important role in supporting the successful delivery of clinical research studies while helping ensure compliance with Good Clinical Practice (GCP), applicable regulations, and study requirements. Working closely with Clinical Trial Managers, field CRAs, sites, and cross-functional project teams, you'll contribute to high-quality study execution that supports clinical research and patient-focused outcomes. In this role, you'll serve as a key partner in site management activities, helping maintain study documentation, support monitoring activities, coordinate site communications, and assist with data quality and operational oversight. Your work will help keep studies on track, support investigative sites, and drive the timely achievement of critical project milestones. Where You'll Work This is a REMOTE role open to candidates based in Australia. You will collaborate with global teams across multiple time zones. Travel may be required as needed to support remote monitoring and study-related site activities. What You'll Do Support site start-up activities, including feasibility questionnaire coordination, confidentiality agreement collection, and essential document management. Coordinate the distribution and tracking of study materials to investigative sites and ensure accurate documentation is maintained. Review site documentation for quality and completeness and support Trial Master File (TMF) maintenance and reconciliation activities. Conduct remote monitoring activities and support pre-study, initiation, interim, and closeout visits under the guidance of Clinical Trial Managers and field CRAs. Maintain regular communication with investigative sites, providing operational support and helping resolve study-related questions and issues. Review electronic case report forms and study data for completeness, consistency, and compliance with study requirements. Assist sites with data management queries, vendor-related requests, study recruitment activities, and subject eligibility tracking. Generate study reports, maintain study trackers, and provide operational updates that support effective project oversight and decision-making. Support site personnel changes, training documentation, regulatory document collection, and vendor access management. What You'll Bring A four-year degree with a concentration in medical, biological, physical, health, pharmacy, or another related science field preferred; alternatively, equivalent education, training, and relevant clinical research experience. Clinical research experience in roles such as Study Coordinator, Clinical Trial Assistant, or other relevant research positions. Understanding of clinical research principles, processes, and Good Clinical Practice (GCP) requirements. Knowledge of FDA and/or EU regulations, ICH Guidelines, local regulatory requirements, and standard operating procedures. Familiarity with electronic data capture (EDC), eCRF, IVRS, and other clinical research systems. Strong planning, organization, and time management skills with the ability to manage multiple priorities effectively. Excellent communication and interpersonal skills with the ability to collaborate across sites and cross-functional teams. Proficiency in spoken and written English. We love knowing that someone is going to have a better life because of the work we do. To view our other roles, check out our careers page at Discover a world of difference at Worldwide ! For more information on Worldwide, visit www.Worldwide.com or connect with us on LinkedIn . Worldwide is an equal opportunity employer that is committed to enabling professionals from all backgrounds and experiences to succeed and, to that end, we prioritize attracting diverse talent and cultivating an inclusive environment that encourages collaboration and creativity. We know that when our employees feel appreciated and included, they can be more creative, innovative, and successful. We’re on a mission to hire the very best and are committed to creating exceptional employee experiences where everyone is respected and has access to equal opportunity. We provide equal employment opportunities to all employees and applicants regardless of race, color, ethnicity, ancestry, religion, national origin, gender, sex, gender identity or expression, sexual orientation, age, citizenship, marital or parental status, disability, military status, or other class protected by applicable law .
In-House Clinical Research Associate I
Worldwide Clinical Trials · Posted 13 days ago
About the role
Who we are We’re a global, midsize CRO that pushes boundaries, innovates and invents because the path to a cure for the world’s most persistent diseases is not paved by those who play it safe. It is built by those who take pioneering, creative approaches and implement them with quality and excellence. We are Worldwide Clinical Trials, and we are a global team of over 3,500 experts, bright thinkers, dreamers and doers and, together, we are changing the way the world experiences CROs – in the best possible way. Our mission is to work with passion and purpose every day to improve lives and we are looking for others who value this same pursuit. Why Worldwide We believe everyone plays an important role in making a world of difference for patients and their caregivers. From our hands-on, accessible leaders, to our cohesive and supportive teams, we are committed to enabling professionals from all backgrounds and experiences to succeed. We prioritize cultivating a diverse and inclusive environment that continues to promote collaboration and creativity. We are proud to be a workplace where people thrive by being themselves and are inspired to do their best work every day. Join us! Make an Impact as an Inhouse Clinical Research Associate at Worldwide As an Inhouse Clinical Research Associate, you'll play an important role in supporting the successful delivery of clinical research studies while helping ensure compliance with Good Clinical Practice (GCP), applicable regulations, and study requirements. Working closely with Clinical Trial Managers, field CRAs, sites, and cross-functional project teams, you'll contribute to high-quality study execution that supports clinical research and patient-focused outcomes. In this role, you'll serve as a key partner in site management activities, helping maintain study documentation, support monitoring activities, coordinate site communications, and assist with data quality and operational oversight. Your work will help keep studies on track, support investigative sites, and drive the timely achievement of critical project milestones. Where You'll Work This is a REMOTE role open to candidates based in Australia. You will collaborate with global teams across multiple time zones. Travel may be required as needed to support remote monitoring and study-related site activities. What You'll Do Support site start-up activities, including feasibility questionnaire coordination, confidentiality agreement collection, and essential document management. Coordinate the distribution and tracking of study materials to investigative sites and ensure accurate documentation is maintained. Review site documentation for quality and completeness and support Trial Master File (TMF) maintenance and reconciliation activities. Conduct remote monitoring activities and support pre-study, initiation, interim, and closeout visits under the guidance of Clinical Trial Managers and field CRAs. Maintain regular communication with investigative sites, providing operational support and helping resolve study-related questions and issues. Review electronic case report forms and study data for completeness, consistency, and compliance with study requirements. Assist sites with data management queries, vendor-related requests, study recruitment activities, and subject eligibility tracking. Generate study reports, maintain study trackers, and provide operational updates that support effective project oversight and decision-making. Support site personnel changes, training documentation, regulatory document collection, and vendor access management. What You'll Bring A four-year degree with a concentration in medical, biological, physical, health, pharmacy, or another related science field preferred; alternatively, equivalent education, training, and relevant clinical research experience. Clinical research experience in roles such as Study Coordinator, Clinical Trial Assistant, or other relevant research positions. Understanding of clinical research principles, processes, and Good Clinical Practice (GCP) requirements. Knowledge of FDA and/or EU regulations, ICH Guidelines, local regulatory requirements, and standard operating procedures. Familiarity with electronic data capture (EDC), eCRF, IVRS, and other clinical research systems. Strong planning, organization, and time management skills with the ability to manage multiple priorities effectively. Excellent communication and interpersonal skills with the ability to collaborate across sites and cross-functional teams. Proficiency in spoken and written English. We love knowing that someone is going to have a better life because of the work we do. To view our other roles, check out our careers page at Discover a world of difference at Worldwide ! For more information on Worldwide, visit www.Worldwide.com or connect with us on LinkedIn . Worldwide is an equal opportunity employer that is committed to enabling professionals from all backgrounds and experiences to succeed and, to that end, we prioritize attracting diverse talent and cultivating an inclusive environment that encourages collaboration and creativity. We know that when our employees feel appreciated and included, they can be more creative, innovative, and successful. We’re on a mission to hire the very best and are committed to creating exceptional employee experiences where everyone is respected and has access to equal opportunity. We provide equal employment opportunities to all employees and applicants regardless of race, color, ethnicity, ancestry, religion, national origin, gender, sex, gender identity or expression, sexual orientation, age, citizenship, marital or parental status, disability, military status, or other class protected by applicable law .
Research Associate, Real Estate/REITS
Jefferies Financial Group · Posted 15 days ago
About the role
Description Research Associate, Real Estate/REITS Our highly regarded Australian Equities Research team delivers differentiated, high-conviction investment insights to institutional investors across the Australian market. We provide independent, research-driven analysis covering a broad universe of ASX-listed companies across key sectors including Financials, Resources, Energy, Industrials, Consumer, Healthcare, Technology, REITs and Small & Mid-Cap Equities. We are seeking a Research Associate to support the Australian Real Estate Equity Research team through financial modeling, company and industry analysis, thematic research, and client engagement. The ideal candidate is intellectually curious, analytically rigorous, highly accountable, and thrives in a fast-paced, deadline-driven environment. Responsibilities Support the Australian Real Estate Equity Research team in delivering high-quality, independent, and objective investment research to institutional investors. Conduct detailed analysis of Australian REITs, property developers, and real estate operating companies, including management teams, asset portfolios, capital structures, and industry trends. Maintain and enhance company financial models, including earnings forecasts, NAV models, DCF valuations, and relative valuation frameworks. Monitor and analyze key sector drivers including property valuations, rental growth, occupancy trends, development pipelines, capital management initiatives, interest rates, and macroeconomic developments. Assist in the preparation of earnings previews and reviews, initiation reports, thematic sector publications, company updates, and other research products. Participate in meetings with company management teams, property tours, site visits, industry conferences, and discussions with industry experts and consultants. Support client interactions by responding to investor inquiries, preparing marketing materials, and assisting with institutional client engagements. Develop and maintain industry databases covering property transactions, valuation metrics, leasing activity, and sector performance benchmarks. Collaborate closely with sales, trading, and research colleagues to deliver timely and actionable insights to clients. Appropriately assess risk when business decisions are made, demonstrating consideration for the firm's reputation, clients, and assets by adhering to applicable regulations, policies, ethical standards, and control procedures. Qualifications Bachelor’s degree in Finance, Accounting, Economics, Real Estate, Commerce, or a related discipline. CFA progress or completion is preferred. 1-3 years of experience in equity research, consulting, investment banking, asset management, commercial real estate, valuation, or a related analytical role. Prior experience covering Australian real estate, REITs, property developers, or real assets is highly desirable. Strong financial modeling, accounting, and valuation skills, including experience with NAV, DCF, and relative valuation methodologies. Understanding of key real estate performance metrics, including FFO, AFFO, NTA/NAV, cap rates, occupancy, leasing spreads, and development returns. Proficiency in Excel, PowerPoint, Bloomberg, FactSet, and other financial databases. Excellent written and verbal communication skills, with the ability to distill complex information into clear investment conclusions. Strong attention to detail, organizational skills, and ability to manage multiple priorities under tight deadlines. Demonstrated intellectual curiosity, commercial awareness, and a collaborative mindset. Jefferies is a leading global, full-service investment banking and capital markets firm that provides advisory, sales and trading, research, and wealth and asset management services. With more than 40 offices around the world, we offer insights and expertise to investors, companies, and governments. At Jefferies, we believe that diversity fosters creativity, innovation and thought leadership through the infusion of new ideas and perspectives. We have made a commitment to building a culture that provides opportunities for all employees regardless of our differences and supports a workforce that is reflective of the communities where we work and live. As a result, we are able to pool our collective insights and intelligence to provide fresh and innovative thinking for our clients. Jefferies is an equal employment opportunity employer, and takes affirmative action to ensure that all qualified applicants will receive consideration for employment without regard to race, creed, color, national origin, ancestry, religion, gender, pregnancy, age, physical or mental disability, marital status, sexual orientation, gender identity or expression, veteran or military status, genetic information, reproductive health decisions, or any other factor protected by applicable law. We are committed to hiring the most qualified applicants and complying with all federal, state, and local equal employment opportunity laws. As part of this commitment, Jefferies will extend reasonable accommodations to individuals with disabilities, as required by applicable law. LI-AS
Research Associate, Real Estate/REITS
Jefferies Financial Group · Posted 15 days ago
About the role
Description Research Associate, Real Estate/REITS Our highly regarded Australian Equities Research team delivers differentiated, high-conviction investment insights to institutional investors across the Australian market. We provide independent, research-driven analysis covering a broad universe of ASX-listed companies across key sectors including Financials, Resources, Energy, Industrials, Consumer, Healthcare, Technology, REITs and Small & Mid-Cap Equities. We are seeking a Research Associate to support the Australian Real Estate Equity Research team through financial modeling, company and industry analysis, thematic research, and client engagement. The ideal candidate is intellectually curious, analytically rigorous, highly accountable, and thrives in a fast-paced, deadline-driven environment. Responsibilities Support the Australian Real Estate Equity Research team in delivering high-quality, independent, and objective investment research to institutional investors. Conduct detailed analysis of Australian REITs, property developers, and real estate operating companies, including management teams, asset portfolios, capital structures, and industry trends. Maintain and enhance company financial models, including earnings forecasts, NAV models, DCF valuations, and relative valuation frameworks. Monitor and analyze key sector drivers including property valuations, rental growth, occupancy trends, development pipelines, capital management initiatives, interest rates, and macroeconomic developments. Assist in the preparation of earnings previews and reviews, initiation reports, thematic sector publications, company updates, and other research products. Participate in meetings with company management teams, property tours, site visits, industry conferences, and discussions with industry experts and consultants. Support client interactions by responding to investor inquiries, preparing marketing materials, and assisting with institutional client engagements. Develop and maintain industry databases covering property transactions, valuation metrics, leasing activity, and sector performance benchmarks. Collaborate closely with sales, trading, and research colleagues to deliver timely and actionable insights to clients. Appropriately assess risk when business decisions are made, demonstrating consideration for the firm's reputation, clients, and assets by adhering to applicable regulations, policies, ethical standards, and control procedures. Qualifications Bachelor’s degree in Finance, Accounting, Economics, Real Estate, Commerce, or a related discipline. CFA progress or completion is preferred. 1-3 years of experience in equity research, consulting, investment banking, asset management, commercial real estate, valuation, or a related analytical role. Prior experience covering Australian real estate, REITs, property developers, or real assets is highly desirable. Strong financial modeling, accounting, and valuation skills, including experience with NAV, DCF, and relative valuation methodologies. Understanding of key real estate performance metrics, including FFO, AFFO, NTA/NAV, cap rates, occupancy, leasing spreads, and development returns. Proficiency in Excel, PowerPoint, Bloomberg, FactSet, and other financial databases. Excellent written and verbal communication skills, with the ability to distill complex information into clear investment conclusions. Strong attention to detail, organizational skills, and ability to manage multiple priorities under tight deadlines. Demonstrated intellectual curiosity, commercial awareness, and a collaborative mindset. Jefferies is a leading global, full-service investment banking and capital markets firm that provides advisory, sales and trading, research, and wealth and asset management services. With more than 40 offices around the world, we offer insights and expertise to investors, companies, and governments. At Jefferies, we believe that diversity fosters creativity, innovation and thought leadership through the infusion of new ideas and perspectives. We have made a commitment to building a culture that provides opportunities for all employees regardless of our differences and supports a workforce that is reflective of the communities where we work and live. As a result, we are able to pool our collective insights and intelligence to provide fresh and innovative thinking for our clients. Jefferies is an equal employment opportunity employer, and takes affirmative action to ensure that all qualified applicants will receive consideration for employment without regard to race, creed, color, national origin, ancestry, religion, gender, pregnancy, age, physical or mental disability, marital status, sexual orientation, gender identity or expression, veteran or military status, genetic information, reproductive health decisions, or any other factor protected by applicable law. We are committed to hiring the most qualified applicants and complying with all federal, state, and local equal employment opportunity laws. As part of this commitment, Jefferies will extend reasonable accommodations to individuals with disabilities, as required by applicable law. LI-AS
Research Associate
University of New South Wales · Posted 18 days ago
About the role
One of Australia’s leading research & teaching universities Vibrant campus life with a strong sense of community & inclusion Enjoy a career that makes a difference by collaborating & learning from the best At UNSW, we pride ourselves on being a workplace where the best people come to do their best work. The School of Psychology at UNSW is the leading Psychology school in Australia. It is located in the Faculty of Science and is recognised nationally and internationally for its excellence in research and teaching. It offers world class undergraduate psychology degrees, as well as postgraduate professional Masters training in Clinical and Forensic Psychology, an online Graduate Diploma program, and a PhD research program with over 120 students. 40 academic staff conduct experimental research in many areas of Psychology, including behavioural and cognitive neuroscience, perception, learning, memory and cognition, as well as health, social, developmental, clinical and forensic psychology. UNSW Psychology is the only School in the southern hemisphere ranked in the top 30 by discipline in the THES, QS and ARWU rankings. The School has well equipped research and teaching facilities and attracts outstanding staff and students from Australia and overseas. UNSW is located 5 km from the centre of Sydney and is close to other research centres, teaching hospitals, transport, shopping, and beaches. For further information about the school please visit www.psychology.unsw.edu.au This position is specifically required to contribute towards a research program leveraging single-cell transcriptomics (snRNAseq) of brain tissue to understand differences in animal behaviour. The successful candidate will conduct independent research and work closely with collaborators. They will also be responsible for contributing to open-source analysis pipelines, and data governance. About the role LEVEL A - $118k - $126k plus 17% Superannuation and annual leave loading Fixed Term – 2 years Full time (35 hours) Specific responsibilities for this role include: Contribute independently and collaboratively to a research project requiring collection, processing, analysis, and interpretation of snRNAseq data. Conduct research (as per the norms of the discipline) and/or enable research teams to create high quality scholarly outputs recognised by peers. Undertake specific research project/s under the guidance of a research leader and contribute to development of research activities. Support the dissemination of research outcomes through appropriate channels and outlets. Undertake discipline-appropriate research activities, e.g. literature reviews, data gathering and/or recording of results using appropriate research methods. Participate in and/or present at conferences and/or workshops relevant to the project as required. Assist with the supervision of research students in the research area where required. Align with and actively demonstrate the Code of Conduct and Values. Cooperate with all health and safety policies and procedures of the university and take all reasonable care to ensure that your actions or omissions do not impact on the health and safety of yourself or others. About the successful applicant (Selection Criteria) A PhD in a relevant discipline and/or relevant work experience. Demonstrated experience collecting, processing, and analysing gene expression data. Strong quantitative and programming skills and experience developing reproducible analysis pipelines and/or open-source tools for large datasets. Experience with behavioural testing in mice and brain tissue collection and processing (e.g. nuclei isolation and fixation) is preferred. Experience working with animal research ethics and a clear understanding of regulatory and data-governance requirements in neuroscience research. Demonstrated ability to undertake high quality academic research and conduct independent research with limited supervision. Demonstrated ability to work in a team, collaborate across disciplines and build effective relationships. Evidence of highly developed interpersonal and organisational skills. Evidence of engagement with open-science practices, including code and/or data sharing and the use of open, reproducible workflows Proven commitment to proactively keeping up to date with discipline knowledge and developments. An understanding of and commitment to UNSW’s aims, objectives and values in action, together with relevant policies and guidelines. Knowledge of health and safety responsibilities and commitment to attending relevant health and safety training. You should systematically address the selection criteria listed within the position description in your application. Please apply online - applications will not be accepted if sent to the contact listed. Contact: Philip Jean-Richard-dit-Bressel E: [email protected] Applications close: November 9 th , 2026 Find out more about working at UNSW at www.unsw.edu.au UNSW is committed to equity diversity and inclusion. Applications from women, people of culturally and linguistically diverse backgrounds, those living with disabilities, members of the LGBTIQ community; and people of Aboriginal and Torres Strait Islander descent, are encouraged. UNSW provides workplace adjustments for people with disability, and access to flexible work options for eligible staff. The University reserves the right not to proceed with any appointment.
Senior Clinical Research Associate (Contract)
On Q Recruitment · Posted 18 days ago
About the role
Our client, a clinical-stage biotech company, is seeking an experienced Senior Clinical Research Associate to support a Phase II respiratory study across Australia and New Zealand. As the Sponsor representative, you will act as the lead monitor across an eight-site Phase IIa study, working closely with investigative sites and the CRO partner to provide senior-level oversight from site activation through to close-out, ensuring data quality, protocol compliance, and effective study execution. This role is suited to a highly autonomous CRA who is comfortable operating independently, building strong site relationships, and exercising sound judgement on study and site issues. About You Solid years' CRA monitoring experience, including Phase II studies. Strong knowledge of ICH-GCP and the ANZ clinical trial landscape. Able to work independently and confidently manage site issues and escalations. Life Sciences, Nursing, Pharmacy or related qualification. Willingness to travel across Australia and New Zealand. What's on Offer Flexible independent contractor engagement. Competitive day rate. Opportunity to work directly with senior clinical leadership. Exposure to an innovative respiratory development program with a growing biotech organisation. Apply now through On Q Recruitment for a confidential discussion.
Clinical Research Associate II
PSI CRO · Posted 19 days ago
About the role
Company Description We are the company that cares – for our staff, for our clients, for our partners and for the quality of the work we do. A dynamic, global company founded in 1995, we bring together 3000 driven, dedicated and passionate individuals. We work on the frontline of medical science, changing lives, and bringing new medicines to those who need them. PSI’s business is about conducting clinical research of novel medications. We work at the interface of R&D, pharmaceutical industry and healthcare science and provide services to big and mid-sized pharmaceutical companies. We help our clients to generate data about safety and efficacy of medications and bring the best ones to market. By conducting global clinical research trials, PSI makes cutting-edge treatment available in drugstores all over the world and helps patients with serious medical conditions to improve or even save their life. Help us to make sure that PSI medical and business documents are clear to patients, physicians, regulatory authorities, and clients. We offer an inspiring story of the company that has grown organically from a handful of countries to global presence. PSI is a mature company with standards and practices, but we do not stand still. Every day, there is a figurative Everest to climb, and you will not get bored here. Job Description We’re searching for a knowledgeable, team-oriented CRA II to manage the clinical aspects of full-service global projects in Australia. As a CRA II at PSI, you will work on the frontline of communication with project stakeholders, ensuring timelines, targets and standards of clinical research projects in a variety of therapeutic indications. You will build and maintain relationships with clinical sites and investigators. You will focus on subjects’ rights, safety and well-being and quality of data compliance. You will: Conduct and report all types of onsite monitoring visits Be involved in study startup Perform CRF review, source document verification and query resolution Facilitate site budgets and contract negotiations Monitor trial progress on the country level Be responsible for site communication and management Be a point of contact for in-house support services and vendors Communicate with internal project teams regarding study progress Participate in feasibility research Support regulatory team in preparing documents for study submissions Qualifications College/University degree in Life Sciences, Pharmacy, RN or an equivalent combination of education, training & experience At least 2 years of independent on-site monitoring experience in Australia Experience in all types of monitoring visits in Phase II and/or III Experience in Inflammatory Bowel Disease, Oncology, Infectious Diseases is a plus Full working proficiency in English PC skills to be able to work with MS Word, Excel and PowerPoint Ability to plan, multitask and work in a dynamic team environment Communication, collaboration, and problem-solving skills Ability to travel Additional Information What you’ll get: Competitive salary We offer hybrid work arrangement - 2 days flexi and 3 days in office Access to a wide range of employee benefits such as onsite Gym access Additional 5 days of wellness leave Development and learning opportunities Chance to make a real impact in a meaningful industry About Us PSI is a passionate, organically grown, and award-winning full-service CRO who dares to be different. As a dynamic and global company, we bring together more than 3000 driven and dedicated experts across 60 countries working collectively to help make a positive impact on patient lives. How are we different? PSI is privately owned by the very people who founded the company 30 years ago, and they’re still working here today. As a result, we have grown organically around the globe and have kept our company fully independent, giving us significant advantages and freedoms. Being a Part of the Team As a part of the PSI team, you will have a fair degree of ownership and autonomy to make nuanced country-and department-specific adjustments while nurturing the global PSI culture that unites us across six continents. You will receive continuous support from your global peers and join a fast-paced, innovative, and results-oriented working environment with lean communication lines. We pride ourselves on being approachable, receptive to new ideas, and open to feedback. Growth Opportunities PSI is proud to invest in our people, from entry-level team members to senior leaders, helping you identify and hone your unique strengths at every step of your career. From on-the-job learning experiences to formal development programs, our professionals have a variety of opportunities to continue to grow throughout their career.
Senior Clinical Research Associate (FSP)
Healthcare Professionals Group · Posted 19 days ago
About the role
Benefits Competitive salary package with performance-based incentives. Dedicated FSP model offering long-term sponsor exposure. Flexible working arrangements with a combination of site and office-based activities. Career development opportunities within an established global CRO. About the Company Join a leading Contract Research Organisation (CRO) with an established presence across Australia and the broader Asia-Pacific region. Partnering with pharmaceutical and biotechnology companies, the organisation delivers high-quality clinical research services across a diverse range of therapeutic areas. With a strong reputation for operational excellence and continued investment in its people, the business offers an environment where experienced clinical research professionals can further develop their expertise while contributing to innovative clinical development programs. About the Opportunity An opportunity exists for an experienced Senior Clinical Research Associate (FSP) to join a growing clinical operations team based in Melbourne. Working within a dedicated Functional Service Provider (FSP) model, you will support clinical trial delivery for an established pharmaceutical sponsor, taking ownership of monitoring activities and building strong relationships with investigative sites. This position offers the opportunity to work autonomously while benefiting from the infrastructure and career development pathways of an established CRO. You will play an important role in maintaining study quality, supporting site performance, and ensuring clinical trials progress in accordance with regulatory requirements. Duties Conduct site selection, initiation, routine monitoring, and close-out visits across assigned clinical studies. Build and maintain effective relationships with investigators and site personnel to support study delivery. Monitor site performance, participant recruitment, and adherence to study protocols. Review clinical trial data and essential documentation to ensure accuracy and regulatory compliance. Provide guidance and training to investigative sites on study procedures and operational requirements. Identify and resolve site-related challenges, escalating quality or operational concerns where appropriate. Prepare monitoring reports and maintain accurate documentation within electronic trial management systems. Collaborate with sponsor representatives and internal clinical operations teams to achieve study milestones. Support site readiness for audits, inspections, and other quality assurance activities. Skills and Experience Minimum four years of independent clinical trial monitoring experience is essential. Previous experience as a Senior Clinical Research Associate within a CRO or pharmaceutical environment. Strong understanding of ICH-GCP guidelines and Australian clinical research regulations. Demonstrated experience independently managing investigative sites throughout the clinical trial lifecycle. Excellent communication and stakeholder management skills, with the ability to engage confidently with investigators and sponsor representatives. Strong organisational skills and ability to manage competing study priorities. Comfortable working autonomously within a field-based monitoring environment. Tertiary qualification in Life Sciences, Nursing, Pharmacy, or a related healthcare discipline is preferred. Culture Join a collaborative, quality-focused organisation where experienced clinical research professionals are encouraged to take ownership of their work. The team values accountability, professional development, and strong stakeholder relationships, offering the support of an established CRO alongside the autonomy of a dedicated sponsor partnership. How to Apply Click apply or contact Rohan Lallbeeharry – Senior Recruitment Consultant – at [email protected] or call 61 485 860 660 for a confidential discussion. About Healthcare Professionals Group Healthcare Professionals Group recruits all positions: executive, permanent, contracting/temp, at all levels, across all areas of healthcare - Pharmaceuticals, Biotechnology, Medical Technology and Clinical Care. Medical Affairs & Life Sciences Recruitment - Clinical Research, Market Access, Medical Affairs, Pharmacovigilance, Quality, Data Management, Regulatory Affairs, Scientific; Commercial Recruitment - Marketing, Sales, Analytics, Government and External Affairs; Business Operations & Infrastructure Recruitment - Administration, Customer Service, Engineering, Finance, Human Resources, IT, L&D, Legal, Manufacturing, Operations, Supply Chain, Warehouse; Clinical Care Recruitment - Allied Health, Aged Care, General Practice, Medical Imaging, Medical Management, Medical Specialties, Nursing.
Senior Clinical Research Associate
Healthcare Professionals Group · Posted 20 days ago
About the role
About the company Join a well-established Australian CRO with a strong APAC footprint, delivering trials across multiple therapeutic areas and all phases. You'll be part of a close-knit team that values your input and invests in your development. About the opportunity As a Senior CRA, you'll be central to delivering high-quality clinical trials, keeping studies safe, ethical and efficient while building lasting partnerships across sites and sponsors. Duties FSP model Conduct site selection, initiation, interim monitoring and close-out visits Develop and drive patient recruitment plans with sites Train and support site staff on study protocols and materials Perform data checks in line with the Clinical Monitoring Plan Resolve site issues promptly and escalate where needed Follow up on quality issues as they arise Prepare and finalise monitoring visit reports Collect and upload essential documents to the eTMF on time Support investigator selection and feasibility activities Prepare sites for audits and regulatory inspections Skills and Experience Bachelor’s degree in a scientific discipline or health care is preferred Previous experience as a Senior CRA Minimum of 4 years of independent monitoring experience Excellent knowledge of ICH-GCP guidelines and local regulations Understanding of the drug development process Strong written, verbal, and computer skills Ability to work independently in remote environments Culture You'll join a collaborative, high-performing team where ownership is encouraged, ideas are heard and your work makes a real difference to clinical research across Asia-Pacific. How to Apply Click apply or contact Davina Ocansey-Gibson, Specialist Manager on 61 2 8877 8712 for a confidential discussion. About Healthcare Professionals Group Healthcare Professionals Group recruits all positions: executive, permanent, contracting/temp, at all levels, across all areas of healthcare - Pharmaceuticals, Biotechnology, Medical Technology and Clinical Care. Medical Affairs & Life Sciences Recruitment - Clinical Research, Market Access, Medical Affairs, Pharmacovigilance, Quality, Data Management, Regulatory Affairs, Scientific; Commercial Recruitment - Marketing, Sales, Analytics, Government and External Affairs; Business Operations & Infrastructure Recruitment - Administration, Customer Service, Engineering, Finance, Human Resources, IT, L&D, Legal, Manufacturing, Operations, Supply Chain, Warehouse; Clinical Care Recruitment - Allied Health, Aged Care, General Practice, Medical Imaging, Medical Management, Medical Specialties, Nursing. For more job opportunities, visit www.hpgconnect.com.
Clinical Research Associate (CRA)
ICON Clinical Research · Posted 20 days ago
About the role
CRA II Sydney Australia At ICON Strategic Solutions, you will work in a sponsor-dedicated model, supported by ICON's global expertise. As the world's largest FSP organisation, with over 90 sponsor partnerships, we offer stability, career development and a collaborative environment where your work contributes to the development of treatments that benefit patients worldwide. As a CRA II at ICON, you will design and analyse clinical trials, interpreting complex medical data, and contribute to the advancement of innovative treatments and therapies. What You Will Do: You will contribute to clinical trial monitoring activities, taking responsibility for your deliverables and working collaboratively. Key responsibilities include: Conducting site qualification, initiation, monitoring, and close-out visits for clinical trials. Ensuring protocol compliance, data integrity, and patient safety throughout the trial process. Collaborating with investigators and site staff to facilitate smooth study conduct. Performing data review and resolution of queries to maintain high-quality clinical data. Contributing to the preparation and review of study documentation, including protocols and clinical study reports Your Profile: You will bring relevant clinical trial monitoring experience, along with the following qualifications and skills. Required qualifications and experience: Bachelor's degree in a scientific or healthcare-related field. Minimum of 2 years of experience as a Clinical Research Associate. In-depth knowledge of clinical trial processes, regulations, and ICH-GCP guidelines. Strong organizational and communication skills, with attention to detail. Ability to work independently and collaboratively in a fast-paced environment. Willingness to travel as required (approximately 60%) What ICON can offer you: Our success depends on the quality of our people. That's why we've made it a priority to build a diverse culture that rewards high performance and nurtures talent. In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family. Our benefits examples include: Various annual leave entitlements A range of health insurance offerings to suit you and your family's needs. Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead. Global Employee Assistance Programme, LifeWorks, offering 24-hour access to a global network of over 80,000 independent specialized professionals who are there to support you and your family's well-being. Life assurance Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, among others. Visit our careers site (https://careers.iconplc.com/benefits) to read more about the benefits ICON offers. At ICON, inclusion & belonging are fundamental to our culture and values. We're dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know or submit a request here (https://careers.iconplc.com/reasonable-accommodations) Interested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless - there's every chance you're exactly what we're looking for here at ICON whether it is for this or other roles. Are you a current ICON Employee? Please click here (https://wd3.myworkday.com/icon/d/task/1422$1235.htmld) to apply
Research Associate - Astrophotonic Instrumentation
National Research Council Canada · Posted 20 days ago
About the role
Priority may be given to the following designated employment equity groups: women, Indigenous Peoples* (First Nations, Inuit and Métis), persons with disabilities and racialized persons*. * The Employment Equity Act , which is under review, uses the terminology Aboriginal peoples and visible minorities. Candidates are asked to self-declare when applying to this hiring process. City: Victoria Organizational Unit: Herzberg Astronomy and Astrophysics Classification: RO Tenure: Term Duration: 3 years Language Requirements: English Work arrangements: Due to the nature of the work and operational requirements, this position will require full-time physical presence at the NRC work location identified. At the NRC, we recognize that Indigenous candidates may have important connections to their communities and you may be eligible for an exception to this work arrangement. Alternative work arrangements may also be considered to accommodate candidates as required. To learn more about these options, please contact the NRC Hiring team using the contact information below. Discover the possible Anything is possible at the NRC, named in 2026 one of Canada’s Top Employers for Young People, Top Employer in the National Capital Region and Forbes Canada’s Best Employers! As Canada’s largest research and innovation organization, our world-renowned research pushes the boundaries of science and engineering to make the impossible, possible. Every day we explore new ideas through innovative research and help companies discover possibilities that impact Canada’s future and the world. At the NRC, you’ll also discover new possibilities. Our supportive workplace fosters a culture of creativity, welcoming fresh perspectives and innovation at all levels. We value teamwork. You’ll collaborate across multiple fields and with the brightest minds to find creative solutions. Most importantly, you’ll discover what’s possible within you as you grow, make valuable contributions and progress in your professional journey. From ground-breaking discoveries to a life-changing career, discover your possible at the NRC. The role We are seeking an instrumentation scientist or engineer who will play a lead role in the development of new astronomical instrumentation based on fiber optic and photonic chip technologies. The Instrumentation Scientist would be someone who shares our core values of Integrity, Excellence, Respect, and Creativity. The successful candidate will participate in the TESERACT project, a CubeSat mission that will demonstrate a novel type of spectroscopy in space. As a Research Associate in our team, you will contribute to the instrumentation effort based on our photonic integral field unit (IFU) architecture through fiber-coupling, alignment, integration, on-sky and in-lab characterization. The long-term objective is a multi-object spectral characterization instrument for biosignature detection on Earth-like exoplanets, with applications in Earth observation. The work shifts from bulk optics to chip-scale photonic processing, improving size, weight, power, cost, stability, and scalability while maintaining high resolution. Key technical areas include: Integral field unit (IFU) and integral field spectroscopy feed design and integration Fiber-coupling, microlens arrays, and beam-remapping optics Optical design, alignment, and integration of instrument front-ends Photonic device and sub-system characterization at visible and near-infrared wavelengths On-sky commissioning and validation on ground-based telescopes You will collaborate with researchers from NRC’s Quantum and Nanotechnologies Research Center, the University of Toronto, and Queen's University Belfast, with travel to collaborator sites. Screening criteria Applicants must demonstrate within the content of their application that they meet the following screening criteria in order to be given further consideration as candidates: Education Ph.D. in Science or Engineering, or A Master’s degree in an Engineering field with relevant experience. For information on certificates and diplomas issued abroad, please see Degree equivalency Experience Significant experience in at least two of the following areas: astronomical instrumentation hardware development. working with optical fibers. optical design, optical alignment and setting up new optical benchtop systems. design or characterization of photonic chip technologies. The following may be considered as assets: Experience working in an astronomical instrumentation development team. Experience using or developing optical spectrographs, integral field units (IFUs) or adaptive optic systems. Experience with CubeSat or small satellite payloads and space systems engineering. Experience working with lasers, scientific cameras / optical detectors. Experience working with photonic integrated circuits. Significant experience: 2 to 6 years of related experience Condition of employment Reliability Status For a Reliability Status, verification of background information over a period of 5 years is required. Language requirements English Information on language requirements and self-assessment tests Assessment criteria Candidates will be assessed on the basis of the following criteria: Technical competencies Expertise in constructing laboratory optical setups or instrumentation, including optical component selection, system alignment, and conducting sensitive or complex optical measurements. Expertise in optical component and system design using simulation tools such as Zemax, OpticStudio, Code V, or similar. Expertise developing optical instrumentation or devices. Ability to analyze complex data sets and statistical analysis. Knowledge of computer-instrument interfacing and developing software for data acquisition and instrument control. Behavioural competencies Research - Communication (Level 2) Research - Creative thinking (Level 2) Research - Initiative (Level 2) Research - Results orientation (Level 2) Research - Teamwork (Level 2) Competency Profile(s) For this position, the NRC will evaluate candidates using the following competency profile: Research View all competency profiles Compensation Salary range as of July 20th 2025: $83,985 to $116,641. NOTE : Salary determination will be based on a review of the candidate’s expertise, outcomes and impacts of their previous work experience relative to the requirements of the level. As a guide, the current annual PhD recruiting rate is $83,985. NRC employees enjoy a wide-range of competitive benefits including a robust pension plan, comprehensive health and dental coverage, disability and life insurance, office closure at the end of December, and additional supports to enhance your well-being throughout your career and beyond. About the Herzberg Astronomy and Astrophysics Research Centre We are Canada's gateway to the stars. At the Herzberg Astronomy and Astrophysics Research Centre, we maintain and operate Canada's largest and most powerful observatories and represent the country in some of the world's leading astronomy initiatives. We are astronomy and astrophysics experts, conducting cutting-edge research, operating Canada's national observatories, providing extensive data management and analysis tools through our Canadian Astronomy Data Centre, supporting activities at international observatories and developing advanced astronomical instruments with industrial partners. More… About DAO The Dominion Astrophysical Observatory (DAO) offers capabilities in optical imaging, spectroscopy and spectropolarimetry, and currently operates two research telescopes: the 1.8-metre Plaskett Telescope and the 1.2-metre telescope, which features the high resolution McKellar spectrograph. The DAO conducts technology research and development associated with instrumentation, facility design and construction projects of the domestic, international and future telescopes they support. The Observatory has been designated a national historic site because of its important role in establishing Canada's international scientific reputation in astronomy. Over the decades, these telescopes have contributed significantly to our understanding of the rotation, size and mass of the Milky Way, and of the rarefied interstellar medium between the stars. Recent projects include orbital determination of comets and asteroids, spectroscopy of magnetic stars, and ongoing studies of distant quasars and galaxies. More Notes Relocation assistance will be determined in accordance with the NRC's directives. A pre-qualified list may be established for similar positions for a one-year period. Preference will be given to Canadian citizens and permanent residents of Canada. Please include citizenship information in your application. The incumbent must adhere to safe workplace practices at all times. We thank all those who apply, however only those selected for further consideration will be contacted. Please direct your questions, with the requisition number (26053) to: E-mail: [email protected] Telephone: 343-548-2032 Closing Date: 4 November 2026 - 23:59 Eastern Time For more information on career tools and other resources, check out Career tools and resources *If you are currently a term or continuing employee at NRC, please apply through the SuccessFactors Careers module from your NRC computer.
Senior Clinical Research Associate
PSI CRO · Posted 21 days ago
About the role
Job Description We’re searching for a knowledgeable, team-oriented Senior CRA to manage the clinical aspects of full-service global projects in Australia. As a Senior CRA at PSI, you will work on the frontline of communication with project stakeholders, ensuring timelines, targets and standards of clinical research projects in a variety of therapeutic indications. You will build and maintain relationships with clinical sites and investigators. You will focus on subjects’ rights, safety and well-being and quality of data compliance. Training, mentoring and supervising study level responsibilities for Jr. CRAs Preparation, conduct, and reporting of selection, initiation, routine and closeout monitoring visits Delivering training of investigators, site staff and project teams Work with complex studies Perform CRF review, source document verification and query resolution Be responsible for site communication and management Be involved in site identification process Contact for clinical investigators, vendors and support services in regard to study progress Participate in feasibility research Preparation and delivering of presentations at Investigator’s Meetings Preparation for and attendance at company’s audits; resolution of audit findings Support to Regulatory Affairs in procurement of site regulatory documents Maintenance of study-specific automated tracking systems
Clinical Research Associate (CRA)
IRE · Posted 21 days ago
About the role
CRA II Sydney Australia At ICON Strategic Solutions, you will work in a sponsor-dedicated model, supported by ICON’s global expertise. As the world’s largest FSP organisation, with over 90 sponsor partnerships, we offer stability, career development and a collaborative environment where your work contributes to the development of treatments that benefit patients worldwide. As a CRA II at ICON, you will design and analyse clinical trials, interpreting complex medical data, and contribute to the advancement of innovative treatments and therapies. What You Will Do: You will contribute to clinical trial monitoring activities, taking responsibility for your deliverables and working collaboratively. Key responsibilities include: Conducting site qualification, initiation, monitoring, and close-out visits for clinical trials. Ensuring protocol compliance, data integrity, and patient safety throughout the trial process. Collaborating with investigators and site staff to facilitate smooth study conduct. Performing data review and resolution of queries to maintain high-quality clinical data. Contributing to the preparation and review of study documentation, including protocols and clinical study reports Your Profile: You will bring relevant clinical trial monitoring experience, along with the following qualifications and skills. Required qualifications and experience: Bachelor's degree in a scientific or healthcare-related field. Minimum of 2 years of experience as a Clinical Research Associate. In-depth knowledge of clinical trial processes, regulations, and ICH-GCP guidelines. Strong organizational and communication skills, with attention to detail. Ability to work independently and collaboratively in a fast-paced environment. Willingness to travel as required (approximately 60%) Employment with ICON is contingent upon having the legal right to work in the country where the role is based. Rewards & Benefits ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development. Benefits may include: Competitive base salary and performance related incentives Health and wellbeing programmes including medical, dental, and vision coverage where applicable Retirement and pension plans Life assurance and disability coverage Employee assistance programmes and wellbeing resources Learning and development opportunities through structured training and career pathways Benefits may vary depending on role and location. Visit our careers site to read more about the benefits ICON offers. Inclusion and Accessibility ICON is an equal opportunity employer. We are committed to building an inclusive and accessible workplace where everyone feels valued and supported. If you require reasonable accommodations during the recruitment process, please let us know or submit a request here . Are you a current ICON Employee? Please click here to apply
Postdoctoral Research Associate (Pharmacy Practice Research)
University of Sydney · Posted 21 days ago
About the role
Part-time, fixed-term position for 12 months Help development and delivery of innovative pharmacy practice research focused on improving healthcare outcomes Base Salary starting from $113,634 17% Superannuation About the opportunity The Sydney School of Pharmacy is one of Australia's leading centres for pharmacy education and research, with a long-standing reputation for excellence in pharmaceutical sciences, pharmacy practice, medicines optimisation, and health services research. Located within the University of Sydney's vibrant Camperdown campus, the School is committed to improving health outcomes through innovative research, strong industry and healthcare partnerships, and the development of the next generation of pharmacy professionals. Our researchers work collaboratively across disciplines to address complex healthcare challenges and deliver real-world impact for patients, clinicians, and communities. An exciting opportunity exists for a Postdoctoral Research Associate ( Level A) (Pharmacy Practice Research) to join the Sydney School of Pharmacy and contribute to an NHMRC Investigator Grant research program. This position will support the development and delivery of innovative pharmacy practice research focused on improving healthcare outcomes through evidence-based interventions and stakeholder engagement. Working closely with the Chief Investigator and research team, the successful candidate will play a key role in the co-design of research with clinicians and people with lived experience, preparation of ethics applications, and establishment of a randomised controlled trial. This position offers an excellent opportunity for an early career researcher to develop their research profile while working on a nationally significant research program. This is a part-time, fixed-term position for 12 months based at the University of Sydney's Camperdown campus. Your key responsibilities will be to : Coordinate and manage research projects to ensure milestones, timelines, and deliverables are achieved undertake qualitative and co-design research activities with clinicians and consumers prepare and submit human research ethics applications and study documentation assist with the establishment and implementation of a randomised controlled trial liaise and collaborate with clinicians, researchers, stakeholders, and people with lived experience contribute to the preparation of research publications and dissemination activities support the development of competitive grant applications assist with mentoring and supporting higher degree research students and junior researchers contribute to a collaborative and productive research environment. About you PhD in Pharmacy, Public Health, Health Services Research, Psychology, Allied Health, or a related discipline (or a PhD submitted and awaiting conferral) experience leading or coordinating research projects demonstrated experience in preparing research manuscripts for publication strong understanding of qualitative research methodologies excellent project management and organisational skills, with the ability to manage competing priorities strong stakeholder engagement and relationship management skills excellent written and verbal communication skills the ability to work both independently and collaboratively as part of a multidisciplinary research team an interest in mentoring students and contributing to a positive research culture. To keep our community safe, please be aware of our COVID safety precautions which form our conditions of entry for all staff, students and visitors coming to campus. Work Rights You must have unrestricted work rights in Australia for the duration of this employment to apply. Visa sponsorship is not available for this appointment. Pre-employment checks Your employment is conditional upon the completion of all role required pre-employment or background checks in terms satisfactory to the University. Similarly, your ongoing employment is conditional upon the satisfactory maintenance of all relevant clearances and background check requirements. If you do not meet these conditions, the University may take any necessary step, including the termination of your employment. EEO statement At the University of Sydney, our shared values include diversity and inclusion and we strive to be a place where everyone can thrive. We are committed to creating a University community that reflects the wider community that we serve. We deliver on this commitment through our people and culture programs, as well as key strategies to increase participation and support the careers of Aboriginal and Torres Strait Islander People , women , people living with a disability, people from culturally and linguistically diverse backgrounds , and those who identify as LGBTIQ . We welcome applications from candidates from all backgrounds. How to apply Applications (including a cover letter, CV, and any additional supporting documentation) can be submitted via the Apply button at the top of the page. For employees of the University or contingent workers, please login into your Workday account and navigate to the Career icon on your Dashboard. Click on USYD Find Jobs and apply. For a confidential discussion about the role, or if you require reasonable adjustment or any documents in alternate formats, please contact Rachel Ann Yazigi, Recruitment Operations by email to [email protected]. © The University of Sydney The University reserves the right not to proceed with any appointment. Click to view the Position Description for this role. Applications Close Sunday 08 November 2026 11:59 PM
Clinical Research Associate - WA/SA
Novotech · Posted 21 days ago
About the role
Description The Clinical Research Associate (CRA), is primarily responsible for ensuring the rights and wellbeing of trial participants are protected and the reported trial data are accurate, complete, and verifiable from the source documents. The CRA is the primary contact between the Investigational Sites, Novotech and Sponsor. Key responsibility of a CRA is as a site relationship manager ensuring that clinical trials are conducted in accordance with ICH GCP guidelines, local and global regulatory requirements, and Novotech/Client SOPs. This role will be based in Perth, and we offer hybrid working arrangements and full flexibility in working hours to ensure our staff achieve the work-life balance often missing in this role. Minimum Qualifications & Experience Graduate in a clinical or life sciences-related field. Relevant experience/qualifications in allied professions may also be considered. Must have good time management skills, attention to detail, be able to work well in a team, and be computer literate. For our current opportunities we require experience of working in the research, pharmaceutical industry or a related field per job level as follows: CRA II: minimum of 6 months of CRA independent monitoring experience CRA III: 2 years of CRA independent monitoring experience You must have full unrestricted working rights in Australia to be considered for this role . We unfortunately cannot provide sponsorship for this role. Responsibilities: CRAs primary responsibility is to build relationships with Principal Investigators, study coordinators, pharmacists, and all relevant site trial personnel to ensure the efficient, expedited and smooth management of clinical trials. Foster internal and external customer relationships to ensure focus on efficient, timely and productive project delivery as per study requirements and timelines. collaboration with the In-house Clinical Research Associate (IHCRA) and Regulatory Start Up Associate (RSA), prepare site essential documents, and support the ethics and regulatory submission and approval processes as needed. In collaboration with Regulatory Start-up (RSU) Team, understand the requirements of applicable local and international regulatory requirements as relevant to specific clinical trials. Ensure recruitment of participants as per the site target. Drive site recruitment and engagement initiatives and prepare site-specific recruitment plan(s) and update as required. Monitoring of investigational sites as per ICH GCP This includes all monitoring visit types across all phases of a clinical trial including Site Selection, Site Initiation, Site Monitoring and Site Close Out, unblinded pharmacy visits, and co-monitoring visits. Visits can be conducted either onsite or remote as per CMP. Responsibilities: CRAs primary responsibility is to build relationships with Principal Investigators, study coordinators, pharmacists, and all relevant site trial personnel to ensure the efficient, expedited and smooth management of clinical trials. Foster internal and external customer relationships to ensure focus on efficient, timely and productive project delivery as per study requirements and timelines. collaboration with the In-house Clinical Research Associate (IHCRA) and Regulatory Start Up Associate (RSA), prepare site essential documents, and support the ethics and regulatory submission and approval processes as needed. In collaboration with Regulatory Start-up (RSU) Team, understand the requirements of applicable local and international regulatory requirements as relevant to specific clinical trials. Ensure recruitment of participants as per the site target. Drive site recruitment and engagement initiatives and prepare site-specific recruitment plan(s) and update as required. Monitoring of investigational sites as per ICH GCP This includes all monitoring visit types across all phases of a clinical trial including Site Selection, Site Initiation, Site Monitoring and Site Close Out, unblinded pharmacy visits, and co-monitoring visits. Visits can be conducted either onsite or remote as per CMP.
Clinical Research Associate
OPIS · Posted 22 days ago
About the role
The Clinical Research Associate is responsible for managing and monitoring clinical trials to ensure they are conducted in compliance with study protocols, ICH-GCP, and applicable regulations. This includes site selection, initiation, monitoring, and close-out activities, while ensuring data quality and patient safety. The role reports to the Clinical Project Manager. Key Responsibilities Identify, assess, and initiate investigational sites Conduct feasibility, pre-study, initiation, monitoring, and close-out visits Ensure compliance with protocols, SOPs, ICH-GCP, and regulatory requirements Perform source data verification and ensure data accuracy and completeness Monitor patient recruitment and support sites in meeting targets Ensure proper reporting of adverse events and protocol deviations Manage investigational product handling, storage, and accountability Maintain study documentation (TMF/eTMF, Investigator Files) Write monitoring reports and follow-up communications Collaborate with project teams, sponsors, and site staff Support audits/inspections and mentor junior CRAs Requirements Degree in a scientific field Minimum 2 years’ CRA or clinical trial monitoring experience Strong knowledge of ICH-GCP, ISO14155, and clinical trial processes Good English and Microsoft Office skills Strong organizational, communication, and problem-solving abilities Ability to work independently and in a team What we offer We offer a competitive salary with other benefits/bonuses and opportunity to develop your professional career with an expanding and growing company. Please read the information notice on the processing of personal data in the candidates information section of our company website. Who we are Founded in 1998 in Italy and now operating at an international level, OPIS is a full-service science driven biotech focused CRO providing premium trial management for multi-country clinical trials, including state-of-the-art information technology solutions and innovative approaches to the increasing complexity and variety of current projects. OPIS added value lies in its highly specialized professionals who can assist their clients using their deep know-how and experience to guarantee a top-quality level of Clinical Trial Management and ability to operate in a wide range of fields (medical writing, scientific and statistical consultancy for trial design, regulatory activities, pharmacovigilance, etc.) always contributing to our clients’ challenging achievements. This page is hosted by JazzHR and uses cookies for technical and analytical purposes. For details regarding the processing of your application data by OPIS, please refer to our: Pivacy Policy Candidate Privacy Policy
Clinical Research Associate II
Premier Research · Posted 22 days ago
About the role
Premier Research is looking for a Clinical Research Associate II to join our Clinical Monitoring, Site Management and SSU team. You will help biotech, medtech, and specialty pharma companies transform life-changing ideas and breakthrough science into new medicines, devices, and diagnostics. What we do is profoundly connected to saving and improving lives, and we recognize our team members are the most valuable asset in delivering success. We are here to help you grow, to give you the skills and opportunities to excel at work with the flexibility and balance your life requires. Your ideas influence the way we work, and your voice matters here. As an essential part of our team, you help us deliver the medical innovation that patients are desperate for. Join us and build your future here. What you'll be doing: Deliver quality, timely monitoring reports for sponsor approval per the Clinical Monitoring Plan timelines Maintain submission of expenses according to travel and expense requirements within company guidelines Monitor (remote, onsite, or other approved mode of monitoring) with a focus on data integrity and patient safety in accordance with specific country regulations Plan day-to-day activities for monitoring of a clinical study and sets priorities per site Prepare for and conducts on-site qualification, study initiation, interim monitoring, and close-out monitoring visits at investigator sites as required by clinical monitoring plan Maintain Trial Master File (TMF)/electronic Trial Master File (eTMF) as defined by the organization’s processes per filing guidelines. Understand the required essential documents according to ICH/GCP Section 8. Review site documents and verifies they are accurate, complete, current, and include required updates What we are searching for: Undergraduate degree or its international equivalent in clinical, science, or health-related field from an accredited institution; a licensed health-care professional (i.e., registered nurse); or equivalent work experience required Previous experience as a CRA required This position requires current working rights for Australia.