Casual Doctors

Canopy Clinical Research; Melbourne; Sur place; AUD 165 000 - 248 000; Temps partiel

Résumé du poste

Canopy Clinical Research in Melbourne is seeking a Casual Doctor to join our site as a Sub-Investigator. You will contribute to safe, compliant conduct of clinical trials while working flexibly alongside your existing practice.

The role emphasizes participant safety, protocol understanding, and collaboration with Nurses, CRAs, Lab Technicians and Administration staff. Training provided and regulation-compliant operations are ensured.

Qualifications

• MBBS or equivalent medical degree completed.
• General Registration with at least 3 years post-graduate experience.
• Current, unconditional AHPRA registration.
• Current GCP certification.
• Professional indemnity insurance.
• Experience in clinical trials preferred but not essential; training provided.
• Strong attention to detail and participant safety.
• Ability to work flexibly across varying study schedules.

Responsabilités

• Conduct participant screening, assessments, and follow-up visits according to study protocols.
• Understand study protocol, investigator’s brochure and informed consent form (ICF).
• Maintain clinical oversight of medical care, procedures and decisions for the study.
• Assist with other trial roles (e.g., phlebotomy, ECGs, nasal swabs).
• Perform medical evaluations and determine eligibility.
• Review adverse events and serious adverse events.
• Provide medical oversight and sign off on trial documentation.
• Ensure compliance with ICH GCP guidelines and applicable legislation.
• Collaborate with site clinical and coordination teams (nurses, CRAs, lab staff).

Connaissances

Attention to detail

Flexible scheduling

Clinical trial understanding

Formation

MBBS or equivalent medical degree

General Registration (3 years minimum)

Description du poste

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