Clinical Investigator Medical jobs
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- Orygen, The National Centre of Excellence in Youth...Parkville VIC
- Salary packaging
- Transportation links
- End-to-end clinical operations - Support studies from start-up and Investigational Product set-up through to eCRF/data management and post-approval reporting.
- If applicable, may be accountable for site financial management according to executed clinical trial agreement and retrieve invoices according to local…
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View similar jobs with this employerIQVIASydney NSW- Health insurance
- If applicable, may be accountable for site financial management according to executed clinical trial agreement and retrieve invoices according to local…
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- サイネオス・ヘルスSouth Australia
- Employee rewards program
- Participates in global clinical monitoring/project staff meetings (inclusive of Sponsor representation, as applicable) and attends clinical training sessions…
- Thermo Fisher ScientificSydney NSW
- Parental leave
- Employee assistance program
- Paid volunteer leave
- Birthday leave
- Representing the organization in the global medical research community, you may develop collaborative relationships with investigators and site personnel to…
- ParexelRemote
- Support the study clinician in ensuring patient safety, eligibility and providing clinical guidance to investigators.
- Support database release as needed.
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- Arrowhead PharmaceuticalsAustralia
- Support company sponsored clinical trials through investigator site engagement.
- Ability to identify the unmet medical, educational, and research needs at a…
- ParexelRemote
- Support the study clinician in ensuring patient safety, eligibility and providing clinical guidance to investigators.
- Support database release as needed.
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View similar jobs with this employerサイネオス・ヘルスSouth Australia- Employee rewards program
- Participates in global clinical monitoring/project staff meetings (inclusive of Sponsor representation, as applicable) and attends clinical training sessions…
Clinical Trial Coordinator
Often replies in 1 dayKG TalentSydney NSW 2000- Schedule participant visits and coordinate investigator and research nurse availability.
- Coordinate day-to-day activities across multiple clinical trials.
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Clinical Research Associate II
Often replies in 1 dayPSI CROSydney NSW- Onsite gym
- You will build and maintain relationships with clinical sites and investigators.
- As a CRA II at PSI, you will work on the frontline of communication with…
- Alfred HealthAustralia
- Health insurance
- Insurance services
- Salary packaging
- Onsite gym
- AHPRA medical registration without conditions, undertakings or reprimands.
- The Dermatology Research Unit at The Alfred is one of the major Dermatology clinical…
- University of MelbourneAustralia
- Parental leave
- Health insurance
- Employee assistance program
- Salary packaging
- Demonstrate expert knowledge of ICH GCP, NHMRC clinical trial policies and Australian research governance requirements.
- University of MelbourneAustralia
- Parental leave
- Health insurance
- Employee assistance program
- Salary packaging
- Demonstrate expert knowledge of ICH GCP, NHMRC clinical trial policies and Australian research governance requirements.
- Pharming GroupAustralia
- Lead medical affairs projects, including investigator-initiated studies, grants, and research collaborations.
- Focusing primarily on immunology, APDS (Activated…
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- Harrison.aiSydney NSW
- Experience in clinical program management, clinical development strategy and study design/trial management and reporting within the medical device or…
Job Post Details
Clinical Research Associate - job post
Parkville VIC•Hybrid work
$125,000 - $135,000 a year - Full-time, Contract
You must create an Indeed account before continuing to the company website to apply
Job details
Pay
- $125,000 - $135,000 a year
Job type
- Contract
- Full-time
Location
Parkville VIC•Hybrid work
Benefits
Pulled from the full job description
- Salary packaging
- Transportation links
Full job description
-
Research Parkville, VIC Full time, contract
17/7/2026
- Parkville/hybrid opportunity | Close to public transport
- Full or part time 2-year contract | 0.8-1.0 considered
- Supportive on the job development | Join a passionate team
About Orygen
Orygen is Australia’s Centre of Excellence in Youth Mental Health and the largest translational research organisation dedicated to youth mental health in the world.
For over 30 years, Orygen has led groundbreaking early intervention and developed evidence-based models of care to improve the mental health outcomes of young people aged 12-25.
About the job
The Clinical Research Associate will contribute to and support the regulatory compliance of Orygen research projects to ensure Good Clinical Practice compliance as well as assist in the development and maintenance of the Quality Management System (QMS). A key aspect of this role is to ensure all research projects across Orygen are conducted in accordance with best practice.
Reporting to the Head of Sponsor Operations you will:
The following criteria must be met for consideration for this position:
If you’re ready to make a difference in youth mental health and be part of a collaborative, innovative team, apply now.
For the full position description, visit https://www.orygen.org.au/getmedia/47ef4eef-64d2-4f3c-bcd7-2d9d59c51a33/Sponsor-Operations-Specialist-PD-July-2026-final.pdf.aspx
This is a part or full time (0.8-1.0FTE) 2-year contract.
Applications will close on 2nd August (4pm), unless a suitable candidate is found sooner.
Before applying at Orygen, it’s important to understand that you may encounter sensitive information related to mental health as part of your work. Being aware of this and how it could affect you is essential in deciding if this is the right opportunity for you.
Orygen is committed to providing diverse, equitable and inclusive environments for Staff and anyone connected to Orygen. We strive to continue building a culturally safe workplace where our values underpin the way we work and our commitment to First Nations people of Australia, young people and their families, people with disabilities, LGBTIQA+ people and CALD communities. We strongly encourage applications from First Nations people.
Orygen is a child-safe organisation and is committed to promoting and protecting the safety and well-being of all young people and embedding safeguarding practices into all our programs and services. All employment appointments are subject to holding a valid working with children check and successful police check.
Orygen is Australia’s Centre of Excellence in Youth Mental Health and the largest translational research organisation dedicated to youth mental health in the world.
For over 30 years, Orygen has led groundbreaking early intervention and developed evidence-based models of care to improve the mental health outcomes of young people aged 12-25.
About the job
The Clinical Research Associate will contribute to and support the regulatory compliance of Orygen research projects to ensure Good Clinical Practice compliance as well as assist in the development and maintenance of the Quality Management System (QMS). A key aspect of this role is to ensure all research projects across Orygen are conducted in accordance with best practice.
Reporting to the Head of Sponsor Operations you will:
- Study monitoring & reporting - Act as Sponsor CRA/monitor across Orygen-sponsored studies, from the development of risk-based monitoring plans and site visits through to safety oversight and close-out.
- Regulatory & operations advice - Review study documents and guide Investigators and study teams on regulatory compliance, study design, and best practice.
- Systems & quality assurance - Manage serious breaches and CAPA processes, drive SOP development, and support the eTMF roll-out.
- Research governance - Ensure site activities align with Orygen's Research Governance Framework, helping streamline how research is conducted across Orygen-governed sites.
- End-to-end clinical operations - Support studies from start-up and Investigational Product set-up through to eCRF/data management and post-approval reporting.
The following criteria must be met for consideration for this position:
- Minimum bachelor’s degree or comparable qualification in Science, Life Sciences or other Healthcare-related discipline.
- Extensive background in Pharmaceutical, CRO, Biotech, or academic/medical research settings, with hands-on expertise across study start-up, conduct, and close-out (including Teletrials)
- Strong working knowledge of ICH GCP, safety reporting, and implementation of quality systems including QMS processes.
- Skilled in electronic Case Report Forms (e.g. REDCap), Trial Master File management, and review of protocols, PICFs, and study documentation.
- A collaborative, detail-oriented professional who builds effective relationships across internal and external stakeholders, and thrives under pressure with competing priorities.
- $125,000 - $135,000 pro rata + 12% superannuation and $15,900 in NFP salary packaging + $2,600 meals and entertainment card.
- Embrace the freedom of a hybrid work model, combining remote work with on-site collaboration.
- Make a real impact on young people in a dynamic, youth-centered environment.
- Work in a state-of-the-art facility co-designed with young people to advance youth mental health.
- Support Orygen's mission for youth mental health and contribute to positive social change.
If you’re ready to make a difference in youth mental health and be part of a collaborative, innovative team, apply now.
For the full position description, visit https://www.orygen.org.au/getmedia/47ef4eef-64d2-4f3c-bcd7-2d9d59c51a33/Sponsor-Operations-Specialist-PD-July-2026-final.pdf.aspx
This is a part or full time (0.8-1.0FTE) 2-year contract.
Applications will close on 2nd August (4pm), unless a suitable candidate is found sooner.
Before applying at Orygen, it’s important to understand that you may encounter sensitive information related to mental health as part of your work. Being aware of this and how it could affect you is essential in deciding if this is the right opportunity for you.
Orygen is committed to providing diverse, equitable and inclusive environments for Staff and anyone connected to Orygen. We strive to continue building a culturally safe workplace where our values underpin the way we work and our commitment to First Nations people of Australia, young people and their families, people with disabilities, LGBTIQA+ people and CALD communities. We strongly encourage applications from First Nations people.
Orygen is a child-safe organisation and is committed to promoting and protecting the safety and well-being of all young people and embedding safeguarding practices into all our programs and services. All employment appointments are subject to holding a valid working with children check and successful police check.
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