Medical Doctor

3 weeks ago

City of Melbourne, Australia i-Pharm ConsultingGruppe Full time

Overview

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.

Locations

- Melbourne

- Principal Investigator or Sub-Investigator

- Therapeutic areas: vaccines, respiratory, neurology, cardiovascular, and more

- 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

- Hours: full-time or part-time - anything from 1 day to 4 days per week

- Locations

- Melbourne, Victoria, Australia (On-site)

- Perth, Western Australia, Australia (On-site)

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 kmunday@i-pharmconsulting.com

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