Regulatory and Site Start Up Specialist

Added
16 days ago
Location
Type
Full time
Salary
Salary not provided

Related skills

regulatory affairs clinical trials ich-gcp irb site start-up

📋 Description

  • Deliver site activation readiness on time for assigned sites.
  • Prepare Clinical Trial Applications and submission dossiers.
  • Interact with CA/EC and respond to submissions.
  • Maintain project plans, trackers, and regulatory tools.
  • Coordinate with site CRA to ensure site collaboration.
  • Maintain audit/inspection readiness and TMF filing.
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