Clinical Operations Lead (Clinical Trial Manager)

Added
21 days ago
Type
Full time
Salary
Salary not provided

Related skills

gcp monitoring edc ich site management
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๐Ÿ“‹ Description

  • Oversee CRAs and investigator sites per Monitoring Plan and GCP.
  • Lead regional/global clinical operations and ensure regulatory compliance.
  • Train CRAs and provide guidance on study procedures and timelines.
  • Develop enrollment strategies and monitor site performance.
  • Prepare monitoring plan and track deviations and escalations.
  • Review visit reports and ensure timely, quality deliverables.

๐ŸŽฏ Requirements

  • College diploma/degree and 7-9 years' experience; or undergraduate degree and 4-6 years.
  • Minimum 3 years CRA experience; strong EDC experience.
  • Proficient in MS Office; excellent written and verbal communication.
  • GCP and local regulatory knowledge; ICH guidelines.
  • Health Sciences or Nursing background; SoCRA/ACRP preferred.
  • Proactive, detail oriented, highly organized; strong documentation skills.

๐ŸŽ Benefits

  • Remote/home-based work.
  • Accommodations for persons with disabilities available on request.
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