Clinical Trial Investigator – Full‑time & Part‑time Roles

About the role

We are seeking motivated Medical Doctors to join a leading clinical research organisation. The role involves conducting and overseeing clinical trials across multiple therapeutic areas, ensuring participant safety and high‑quality data collection.

Key responsibilities

• Perform participant assessments and clinical reviews in line with study protocols.
• Maintain participant safety, eligibility, and protocol compliance throughout the trial.
• Review clinical data, pathology reports, and participant results promptly.
• Prepare and keep audit‑ready source documentation following GCP and ALCOA+ principles.
• Support recruitment and retention activities for ongoing trials.
• Collaborate with internal teams, sponsors, and monitoring personnel to ensure successful trial delivery.
• Participate in sponsor visits, monitoring activities, and quality improvement initiatives.

Required profile

• Medical degree with unrestricted AHPRA registration.
• Current medical indemnity insurance.
• Strong understanding of Good Clinical Practice (GCP) and clinical governance.
• Excellent communication and stakeholder engagement abilities.
• Detail‑oriented clinical judgement and a collaborative mindset.

Required skills

What we offer

• Opportunity to work on innovative, impactful clinical trials.
• Supportive, collaborative team culture with strong focus on professional development.
• Exposure to a broad range of therapeutic areas and sponsor organisations.
• Modern research environment with robust operational support.