Research Associate Director

6 days ago


Sydney, New South Wales, Australia George Clinical Pty Full time
Key Responsibilities

You will be responsible for:

  • Verifying the quality, accuracy, completion, and timeliness of data from trial sites.
  • Maintaining trial information using the clinical trial management system.
  • Supporting strategies to boost recruitment efforts.
  • Performing site close-out visits and other site activities as required.
About You

To be successful in this role, you will require:

  • A degree in pharmacy, medical, nursing, biological science, or other health-related disciplines.
  • ≥5 years' experience in clinical trial monitoring and/or site management.
  • High competence in negotiation and conflict resolution, critical thinking, problem-solving, decision making, and strategic thinking.

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