Casual Doctors

About the Company:

Canopy Clinical Research is a dedicated, multi-site, Clinical Trials network on the East-coast of Australia. We conduct trials on a broad therapeutic range, from Phase 1 through to Phase 4. We excel in generalist studies with a large volunteer recruitment pool and have proven to be equally capable in delivering results for more specialist indications requiring patients.

The Role

We are seeking a motivated and experienced Casual Doctor to join our Melbourne team. This is an excellent opportunity for a clinician looking to expand into clinical research, or an experienced investigator seeking flexible, meaningful work alongside their existing practice. You will work as a Sub-Investigator, contributing to the safe and compliant conduct of clinical trials at our site.

Key Responsibilities

• Conducting participant screening, assessments, and follow-up visits in accordance with study protocols

• Understanding of study protocol, investigator’s brochure and informed consent form (ICF)

• Maintain clinical oversight of medical care, procedures and decisions regarding the study.

• Assist with other trial roles when required (eg. phlebotomy, ECGs, nasal swabs, etc).

• Performing medical evaluations and making eligibility determinations

• Reviewing and assessing adverse events and serious adverse events

• Providing medical oversight and signing off on clinical trial documentation

• Ensuring compliance with ICH Good Clinical Practice (GCP) guidelines and applicable legislation

• Collaborating with the site's clinical and coordination team i.e Nurses, Clinical Research Coordinators, Lab Technicians and Administration staff

What We're Looking For

• MBBS or equivalent medical degree

• General Registration post graduate 3 years minimum

• Current, unconditional AHPRA registration

• Current GCP certification (this can be completed prior to commencement)

• Professional indemnity insurance

• Experience in clinical trials preferred, but not essential — training is provided

• Strong attention to detail and a commitment to participant safety

• Ability to work flexibly across varying study schedules