Medical Doctor

5 days ago

Melbourne, Victoria, Australia i-Pharm Consulting Full time $120,000 - $250,000 per year

Medical Doctor | Physician | Principal Investigator | Sub-Investigator

Sydney OR Melbourne - X2 opportunities

I'm looking to connect with medical professionals to join a
private clinical trial site
in either Sydney or Melbourne. At the site, they partner with global pharmaceutical and biotech companies to run clinical research studies. As a doctor here, you'll play a critical role in advancing new treatments while working in a supportive, structured environment that runs more like a private practice than a hospital.

Your role will involve supervising or directly managing clinical trials from start-up through to close-out. Depending on your experience, you will join as either
Principal Investigator (PI)
, responsible for leading and overseeing trials, or as
Sub-Investigator (Sub-I)
, assisting the PI while developing your skills in clinical research.

This role offers a
predictable routine
compared to hospital medicine - standard working hours, no night shifts or on-call requirements, and the opportunity to see patients in a research-focused setting. You will also gain exposure to the business side of research, operating within a private site that collaborates with leading sponsors across a variety of therapeutic areas.

Melbourne

  • Principal Investigator or Sub-Investigator
  • Therapeutic areas: vaccines, respiratory, neurology, cardiovascular, and more
  • Phases I–IV studies
  • Hours: full-time (Mon–Fri) or part-time (3 days/week, flexible)

Sydney

  • Principal Investigator or Sub-Investigator
  • Therapeutic areas: HIV, respiratory, neurology, and more
  • Phases I–IV studies
  • Hours: full-time or part-time - anything from 1 day to 4 days per week

Key Responsibilities

  • Serve as either Principal Investigator or Sub-Investigator on assigned clinical trials
  • Oversee patient safety, medical assessments, and trial protocol compliance
  • Collaborate with study coordinators, nurses, and sponsor representatives
  • Contribute to data accuracy, adverse event reporting, and study timelines
  • Build relationships with industry sponsors and contribute to the site's growth

Experience Required

  • AHPRA-registered medical doctor (specialist or non-specialist)
  • Interest in or prior exposure to clinical trials (training provided for Sub-Is)
  • Strong communication and patient-care skills
  • Ability to work collaboratively in a multidisciplinary environment

This is a great career step for doctors seeking a
stable clinical role in research
with the chance to influence the future of medicine while working in a professional private-site setting.

Contact Keeley Munday at -

LinkedIn:

Or apply directly to this advert.

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