Study Site Coordinator

2 weeks ago

Sydney, New South Wales, Australia beBeeClinicalResearch Full time $80,000 - $120,000

Job Summary:

This role is responsible for overseeing project management and study site management from site selection to initiation, monitoring, and close-out of assigned clinical studies in accordance with applicable regulations.

About the Role
  • Site Management: Study site selection, initiation (SIV), and clinical monitoring.
  • Ensure Principal Investigator/study staff complies with safety reporting requirements.
  • Track study recruitment to ensure the target is achieved.
  • Conduct monitoring visits according to SDV plans and SOPs; address issues with sites and complete monitoring visit reports in a timely manner.


Key Responsibilities:

  • Project Coordination: Coordinate project activities to meet deadlines and deliverables.
  • Clinical Trial Operations: Ensure compliance with Good Clinical Practice and relevant regulatory requirements.
Qualifications:
  • Bachelor's degree or higher in Medical, Pharmacology, or Biology-related majors.
  • At least 1 year of experience in a similar role.
  • Familiarity with clinical trial processes and procedures.

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