You will also act as Principal Investigator for assigned studies and play a key role in mentoring junior physicians and contributing to the successful delivery of clinical research programs.
Key Responsibilities
- Provide medical oversight for clinical trial participants including consent, screening, safety monitoring, and adverse event management.
- Act as Principal Investigator for assigned studies, ensuring trials are conducted in accordance with protocol, GCP, and regulatory requirements.
- Collaborate with recruitment, project, and sponsor teams to support enrolment, protocol delivery, and participant safety.
- Provide medical expertise to project teams, investigators, and external stakeholders including sponsors and medical monitors.
- Mentor and supervise junior Research Physicians while supporting a collaborative and high-quality research environment.
- Medical Degree with current AHPRA registration enabling clinical research practice.
- Experience working in clinical trials, ideally with exposure as a Principal Investigator or Co-Investigator.
- Strong knowledge of ICH-GCP and clinical research regulations.
- Excellent communication skills with the ability to build relationships with sponsors, investigators, and clinical teams.
- Proven ability to manage multiple studies and competing priorities in a fast-paced research environment.
- Opportunity to lead and shape early phase clinical research programs.
- Work alongside an experienced and collaborative medical and clinical operations team.
- Contribute to innovative trials that advance new therapies and improve patient outcomes.
