Clinical Trial Investigator

An established clinical research organisation is seeking a Clinical Trial Investigator to support the delivery of high-quality clinical trials across a diverse portfolio of studies. This role is responsible for ensuring participant safety, protocol compliance, and the delivery of exceptional clinical care while contributing to the successful execution of research projects.

• Conduct participant assessments, eligibility reviews, informed consent, and study visits in accordance with study protocols and Good Clinical Practice (GCP).
• Ensure participant safety through ongoing clinical monitoring and appropriate medical management.
• Maintain accurate, compliant source documentation and clinical records.
• Review clinical data, laboratory results, and adverse events within required timeframes.
• Collaborate with multidisciplinary site teams, sponsors, and stakeholders to support trial delivery and recruitment.
• Participate in monitoring visits, audits, and regulatory activities.
• Contribute to continuous quality improvement, protocol implementation, and operational excellence.

• Registered Medical Practitioner with unrestricted AHPRA registration (General or Specialist).
• Current Medical Indemnity Insurance.
• Australian Citizen or Permanent Resident.
• Strong understanding of Good Clinical Practice (GCP) and clinical research principles.
• Excellent clinical judgement, communication, and stakeholder management skills.
• Highly organised with strong attention to detail and a commitment to participant-centred care.
• Collaborative, adaptable, and committed to delivering high-quality outcomes in a fast-paced research environment.

• Opportunity to work on innovative clinical research that contributes to improving patient outcomes.
• Collaborative and supportive multidisciplinary team environment.
• Ongoing professional development and training.
• Opportunity to work as a Sub-Investigator and/or Principal Investigator, depending on experience and study requirements.