Clinical Research Coordinator Role
We are seeking a highly skilled and experienced professional to coordinate clinical research activities, working closely with Principal Investigators, Co-investigators, and our research team.
Key Responsibilities:
* Ensure the timely start-up and smooth running of allocated trials onsite, documenting and coordinating trial activities.
* Manage recruitment targets and timelines in collaboration with the team lead and local research team.
* Establish relationships with stakeholders, including patients, centre staff, sponsors, and research leads.
* Perform clinical tasks, such as vital signs, ECGs, venepuncture, medication management, and maintain proficiency.
* Process samples, coordinate sample collection and dispatch, and prepare for monitoring visits.
Requirements:
* AHPRA registration with relevant nursing experience.
* Minimum 2 years' experience in clinical research coordination-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.
* High level of initiative, flexibility, and ability to meet deadlines while balancing multiple priorities.
About Our Organisation:
Our organisation is a progressive and passionate team of healthcare professionals and support staff, united by a common purpose: to design care experiences that deliver the best possible life outcomes. By joining us, you will be part of a dynamic team committed to improving cancer care and making a difference in people's lives.