Clinical Trials Coordinator

UniSC

1d•Hybrid

About The Position

As a Clinical Trials Coordinator, you’ll be at the heart of delivering high-quality, compliant clinical trials that contribute to better health outcomes. You will contribute to the coordination and administration of trials assigned to you, keeping them on track, on time, and in line with all relevant regulations, from ICH/GCP guidelines to UniSC CTC procedures. With sound judgement, a practical approach, and strong protocol knowledge, you’ll ensure every detail runs smoothly. This role also offers the opportunity to mentor Clinical Trial Associates and support student placements, making it a rewarding step forward for both leadership and professional growth. Please note, this role requires flexibility to travel to different clinical trial sites, and to work outside standard business hours to support confinement studies and other time-sensitive trial activities. You may also be required to participate in a 24/7 on-call or confinement roster.

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. Note: 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

Contribute to the coordination and administration of designated clinical trials within UniSC CT
Work collaboratively with the CTC team, sponsors, and monitors to ensure the successful conduct and timely completion of clinical trials