Clinical Studies Specialist

4 days ago

Sydney, New South Wales, Australia beBeeResearch Full time $90,000 - $120,000

Clinical Research Coordinator Role Overview

We are seeking a skilled Clinical Research Coordinator to join our team in Sydney. This role is an excellent opportunity for individuals who share our commitment to innovation and working together to drive better life outcomes for patients around the world.

Job Description

Main Responsibilities:

  • Coordinate and deliver direct and indirect care and associated data collection for clinical trials through collaboration with Principal Investigators, Co-investigators, and the research team.
  • Ensure timely start-up and smooth running of allocated trials onsite, documenting and monitoring progress with support from Research Leads, the start-up team, and your clinical lead.
  • Work closely with the team lead and local research team to meet all recruitment targets and timelines.
  • BUILD STRONG RELATIONSHIPS WITH KEY STAKEHOLDERS INCLUDING YOUR TEAM, RESEARCH LEADS, PI, CENTRE STAFF, AND SPONSORS.
  • Perform clinical tasks such as vital signs, ECGs, venepuncture, medication management as deemed competent, 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 practices as they pertain to research.
  • Ensure all research is conducted in accordance with Good Clinical Practice (GCP) Guidelines, study-specific protocols, and all applicable national and international laws and regulations.
Required Skills and Qualifications

Key Requirements:

  • AHPRA registration with relevant nursing experience.
  • Minimum 2 years' experience as a clinical research coordinator in 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 the 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.
  • Express a high level of initiative and flexibility and 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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