
Clinical Trials Professional
7 days ago
We are seeking a skilled Clinical Research Coordinator to lead our research activities in NSW, working closely with Principal Investigators and the research team.
The successful candidate will be responsible for coordinating and delivering clinical research activities, including documentation, monitoring, and data collection for clinical trials.
Key Responsibilities:- Coordinate and deliver clinical research activities, including documentation, monitoring, and data collection for clinical trials.
- Work with the research team to ensure all recruitment targets and timelines are met.
- Build relationships with key stakeholders, including team members, research leads, and sponsors.
- Perform clinical tasks, such as vital signs, ECGs, venepuncture, medication management, and maintain proficiency.
- Process samples, coordinate sample collection, and dispatch as required.
- Prepare for and host monitoring and close-out visits.
- Maintain up-to-date knowledge in regulatory, administrative, and clinical frameworks and current clinical issues and practice as they pertain to research.
- Current AHPRA registration with relevant nursing experience.
- Minimum of 2 years' experience in clinical research coordinator-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 the ability to work both independently and as part of a team.
- High level of initiative and flexibility with the ability to meet deadlines while balancing multiple priorities.
- Knowledge of Good Clinical Practice and applicable national and international laws and regulations.
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