Clinical Trials Professional

1 week ago

Sydney, New South Wales, Australia beBeeResearch Full time $90,000 - $120,000
Clinical Research Coordinator Role

Our organization is seeking a highly skilled and experienced Clinical Research Coordinator to lead clinical research activities across the coordination of direct and indirect care, and associated data collection for clinical trials.

Key Responsibilities:

  • Coordinate the delivery of clinical research activities through the management and execution of tasks, ensuring timely completion and adherence to trial protocols.
  • Collaborate closely with Principal Investigators, Co-investigators, and research teams to ensure smooth start-up and operation of allocated trials on-site.
  • Develop strong relationships with key stakeholders, including research leads, Principal Investigators, centre staff, and sponsors.
  • Perform clinical tasks such as vital signs, ECGs, venepuncture, medication management, as deemed competent, and maintain proficiency in these areas.
  • Ensure accurate and timely data entry, meeting all requirements and deadlines.
  • Process samples, coordinate sample collection and dispatch as required, maintaining high standards of quality control.
  • Prepare for and host monitoring and close-out visits, demonstrating professionalism and attention to detail.
  • Maintain up-to-date knowledge in regulatory, administrative, and clinical frameworks, and current clinical issues and practice as they pertain to research.

Requirements:

  • Current AHPRA registration with relevant nursing experience.
  • Minimum of 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 the ability to work both independently and as part of a team in an effective, proactive, and cooperative manner.
  • 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.

Benefits:

  • Opportunity to work in a dynamic and fast-paced environment, contributing to cutting-edge research.
  • Professional development and growth opportunities, supporting career advancement.
  • Collaborative and supportive team culture, fostering open communication and teamwork.

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