Clinical Trial Doctors - (Pte And Fte Positions Available)

Tardis Group; Adelaide; On-site; AUD 90,000 - 150,000; Full time

Job summary

Tardis Group is seeking a Medical Doctor to join as a Clinical Trial Investigator in Adelaide, SA. You will ensure safe delivery of trials, protocol compliance, and high-quality outcomes while working with sponsors, research teams, and participants.

You will bring unrestricted AHPRA registration, a clinical trials background, and a strong focus on GCP, governance, and patient safety to support ongoing program growth.

Qualifications

• Medical Degree with unrestricted AHPRA registration.
• Experience in clinical trials, research, or participant-based clinical care.
• Strong understanding of GCP and clinical governance principles.
• Current Medical Indemnity Insurance.

Responsibilities

• Conduct participant assessments and clinical reviews in line with study protocols.
• Ensure participant safety, eligibility, and ongoing protocol compliance.
• Review clinical data, pathology, and participant results in a timely manner.
• Maintain accurate and audit-ready source documentation in accordance with GCP and ALCOA+ principles.
• Support recruitment and retention initiatives across clinical trials.
• Collaborate with internal teams and sponsors to ensure successful trial delivery.
• Participate in sponsor visits, monitoring activities, and quality initiatives.
• Contribute to continuous improvement, CAPAs, and operational excellence.

Skills

Communication

Stakeholder engagement

Attention to detail

Collaboration

Education

Medical Degree

AHPRA registration

Job description

An exciting opportunity is available for a motivated and patient-focused Medical Doctor to join a growing and highly regarded clinical research organisation dedicated to advancing global healthcare through innovative clinical trials.

About the Role

As a Clinical Trial Investigator, you will play a key role in the safe and effective delivery of clinical trials, ensuring participant wellbeing, protocol compliance, and high-quality clinical outcomes.

You will work closely with research teams, sponsors, and participants while contributing to the ongoing success and growth of the organisation's clinical research programs.

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, and participant results in a timely manner
• Maintain accurate and audit-ready source documentation in accordance with GCP and ALCOA+ principles
• Support recruitment and retention initiatives across clinical trials
• Collaborate with internal teams and sponsors to ensure successful trial delivery
• Participate in sponsor visits, monitoring activities, and quality initiatives
• Contribute to continuous improvement, CAPAs, and operational excellence

About You

To be successful in this role, you will bring:

• Medical Degree with unrestricted AHPRA registration
• Previous experience in clinical trials (not essential), research, or participant-based clinical care
• Strong understanding of Good Clinical Practice (GCP) and clinical governance principles
• Excellent communication and stakeholder engagement skills
• Exceptional attention to detail and clinical judgement
• A collaborative, adaptable, and solutions-focused mindset
• Current Medical Indemnity Insurance

What's on Offer

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

We would love to hear from you if you have any interest in clinical research and want to contribute to meaningful medical advancements while working in a progressive and supportive environment.

Clinical Trial Doctors - (PTE and FTE positions available) Adelaide, SA, AU