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 delivering safe, high‑quality clinical trials across multiple therapeutic areas, working closely with multidisciplinary teams, sponsors, and participants.

Key responsibilities

• Conduct participant assessments and clinical reviews in line with study protocols.
• Ensure participant safety, eligibility, and ongoing protocol compliance.
• Review clinical data, pathology reports, and participant results promptly.
• Maintain accurate, audit‑ready source documentation following GCP and ALCOA+ principles.
• Support recruitment and retention initiatives for ongoing trials.
• Collaborate with internal teams and sponsors to achieve 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.
• Attention to detail and sound clinical judgement.

Required skills

What we offer

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