Clinical Trials Sub-Investigator (Junior Doctor)

1w1 week ago

Sinclair Dermatology

East Melbourne, AU · Full-time · A$140,000 – A$180,000

About this role

Join Sinclair Dermatology as Clinical Trials Sub-Investigator (Junior Doctor or equivalent) at busy East Melbourne and Pascoe Vale trials sites. DIRECT is Australia's largest dermatology clinical trials site, running 30-40 pharma-sponsored trials across skin and hair conditions. Many have progressed to TGA approval for public access, led by Professor Rod Sinclair.

Work in a stimulating clinic environment with patient visits, supported by Clinical Trials Coordinators and Assistants. Provide medical oversight for study participants, prioritizing safety and well-being. Report to the Unit Head while handling delegated Sub-Investigator responsibilities per protocol.

Be part of a vibrant, motivated team fostering high-performing culture and great work/life balance. Comply with ICH-GCP guidelines and National Statement on Ethical Conduct in Human Research. Rostered for on-call shifts as phone-based emergency contact only, no in-person attendance required.

Permanent full-time or part-time (0.8 FTE) roles available for early 2025 start. Opportunity to work closely with a dermatologist as assistant. Experience in clinical trials or research viewed favorably, supporting career growth in dermatology trials.

Requirements

Medical doctor registered with AHPRA (IMG with current registration welcome)
At least PGY4 with strong interest in dermatology and clinical trials
Experience conducting disease assessments (e.g., PASI, EASI, HS lesion count)
Strong attention to detail
Effective communicator able to work independently and as part of a team
Flexible and able to think on your feet
Multi-tasker with track record of meeting deadlines
Experience in clinical trials or research, especially commercially sponsored, viewed favorably

Responsibilities

Serve as delegated Sub-Investigator on clinical trials
Comply with ICH-GCP guidelines and the National Statement on Ethical Conduct in Human Research
Conduct disease assessments and calculate extent/severity (e.g., PASI, EASI, HS lesion count)
Screen trial participants after assessing protocol inclusion/exclusion criteria and medication washouts
Obtain participant informed consent according to ICH-GCP and the National Statement
Provide medical care and oversight for enrolled study participants
Perform protocol-required activities like interpreting pathology results, ECGs, and adverse events follow-up
Liaise with participant’s local GP/other healthcare personnel on study progress