Clinical Research Coordinator
On-site · Murdoch, Western Australia, Australia
Job Summary
Coordinate and deliver clinical research activities in line with study protocols, Good Clinical Practice (GCP) guidelines, and regulatory requirements. Partner with Principal and Co-Investigators to manage day-to-day trial activities, support study start-up, participant recruitment, study visits, monitoring, and close-out. Maintain accurate study documentation and regulatory files, perform protocol-specific tasks (e.g., vitals, ECGs, venepuncture, sample processing) as competent, and act as a key point of contact for participants, sponsors, and internal stakeholders. Liaise with hospital departments, third-party providers, and sponsor representatives to ensure smooth trial delivery. Prepare for and host monitoring/site visits, complete mandatory and trial-specific training, and contribute to quality, safety, and compliance activities. Willingness to travel interstate if required and ability to work across locations within a fast-paced public hospital research environment.
Required Qualifications
- Undergraduate degree in Science, Nursing, Pharmacy, or a related discipline
- At least two years’ experience in nursing, research, or a scientific setting
- Solid understanding of Good Clinical Practice (GCP) and clinical trial regulations
- Highly organized, detail-focused, able to manage multiple priorities and deadlines
- Strong communication skills and ability to build relationships with stakeholders
- Willingness to travel interstate if required
- Proficient in MS Office and clinical trial software
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