Seeking a skilled Clinical Research Coordinator to manage clinical research activities, coordinate trial start-ups, and ensure smooth running of allocated trials onsite. Key responsibilities include working closely with Principal Investigators, Co-investigators, and the Research Team to conduct clinical research activities, documenting and monitoring trial data, and maintaining up-to-date knowledge in regulatory, administrative, and clinical frameworks.
About the Role
* Coordinate and deliver direct and indirect care for clinical trials.
* Responsible for timely start-up and smooth running of allocated trials onsite.
* Work with the team lead and local research team to ensure all recruitment targets and timelines are met.
* Maintain relationships with key stakeholders, including team members, research leads, PI, Centre staff, and sponsors.
* Perform clinical tasks such as vital signs, ECGs, venepuncture, medication management, and maintain proficiency.
Requirements
* AHPRA registration with relevant nursing experience.
* Minimum 2 years' experience in clinical research co-ordinator-nursing, science or Phase 1 research, Oncology or nuclear medicine with an equivalent undergraduate degree.
* Strong computer literacy with knowledge of clinical trials software and MS Office suite.
* Excellent communication and interpersonal skills with ability to work independently and as part of a team.
Benefits
* Opportunity to work with a vibrant team aligned with providing the best patient experience possible and outcomes.
* Internal and external training and development opportunities.
* Close-knit internal community.
* All employees and their family members have access to free confidential support.
* Enhance your holistic wellbeing with our Full Circle wellbeing program.
* Range of benefits available.