Clinical Trials Coordinator
About The Position
As a Clinical Trials Coordinator, you will play a central role in delivering high-quality, compliant clinical trials that contribute to improved health outcomes. You will lead assigned studies, ensuring they remain on track, on time, and fully aligned with regulatory requirements, including ICH/GCP guidelines and UniSC CTC procedures. With strong protocol knowledge, sound judgement, and a practical, solutions-focused approach, you will ensure trial activities are executed with precision and consistency. This role also provides the opportunity to mentor Clinical Trial Associates and support student placements, offering a meaningful step forward in both leadership and professional development. This role will include work outside of standard business hours and you will be required to participate in a 24/7 confinement rostering. Flexibility to travel to different clinical trial sites is desired.
Requirements
- Completion of a degree qualification in Health, Science, Nursing, or related field with subsequent relevant experience or an equivalent combination of experience and Diploma qualification.
- Registered Nurses must have current registration with AHPRA as a Registered Nurse.
- Enrolled Nurses must be medication administration endorsed and have phlebotomy training and experience.
- Knowledge of ICH Good Clinical Practice and applicable regulations.
- High level computing skills (including databases, clinical trial electronic data entry, word processing and spreadsheets).
- Sound understanding of privacy principals governing health information.
- Ability to work independently and as part of a multidisciplinary team.
Nice To Haves
- Previous Clinical Trial Coordination experience highly regarded.
Responsibilities
- Plan and conduct patient visits, including data collection, laboratory sample processing and shipping, and complex documentation.
- Coordinate the administration and conduct of multiple clinical trials, including study start-up, ethics and regulatory submissions, recruitment, screening and enrolment.
- Maintain compliance with local, State and federal requirements, study protocols and applicable policies and procedures.
- Collaborate with the Clinical Trials Centre team, sponsors, monitors and healthcare professionals to support effective trial delivery, participant engagement, data reporting and timely completion.
Benefits
- Professional development and career pathway opportunities.
- Flexible work arrangements & generous leave options.
- Salary packing options + 17% Super.
- EAP, fitness passport & discounted private health.
Stand Out From the Crowd
Upload your resume and get instant feedback on how well it matches this job.
What This Job Offers
Job Type
Full-time
Career Level
Mid Level
