Clinical Research Site Activation Coordinator

2 weeks ago

North Sydney Council, Australia beBeeClinicalResearch Full time $80,000 - $110,000

Job Opportunity: Site Activation Specialist

This role supports the site activation process for clinical trials, including feasibility assessments, regulatory submissions, and document tracking.

Key Responsibilities
  • Coordinate with internal teams and external sites to ensure timely and compliant study startup and maintenance.
  • Prepare, review, and distribute site documentation (e.g., CDAs, ICFs, regulatory forms).
  • Track and manage site performance metrics and document status.
Qualifications and Skills
  • Bachelor's degree in Life Sciences or related field.
  • Experience:
    • 1–3 years in clinical research or a related field.
    • Familiarity with regulatory and ethics submissions, ICFs, and site documentation.
  • Strong organizational and communication skills.
  • Ability to manage multiple priorities and meet deadlines.

IQVIA is a leading global provider of clinical research services, commercial insights, and healthcare intelligence to life sciences and healthcare industries.

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