Senior Clinical Trial Manager — Remote Global Leader

NCBioImpact

Durham (NC)

Remote

USD 112,000 - 222,000

Full time

4 days ago
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Job summary

Worldwide Clinical Trials is seeking a Senior Clinical Trial Manager to lead site management across the full trial lifecycle, partnering with sponsors, CRAs, and cross-functional project teams to ensure high-quality outcomes. This is a remote role in the United States with travel up to 25%.

You will oversee monitoring activities, drive collaboration, and guide teams to successful study execution in a patient-focused, compliant environment.

Qualifications

  • Bachelor’s or nursing degree required; clinical trial management experience.
  • 4+ years of CRA experience.
  • Ability to travel up to 25%.
  • Experience supporting Internal Medicine clinical trials (IMID, Cardio Metabolic, Rare Disease).
  • Ability to lead remote teams.

Responsibilities

  • Lead clinical site management activities throughout the full study lifecycle.
  • Serve as primary Site Management representative for monitoring and site activities across assigned projects.
  • Act as sponsor-facing contact, building partnerships and ensuring effective communication.
  • Oversee monitoring deliverables to meet study objectives, quality, and budget.
  • Identify and manage out-of-scope activities with proactive communication.
  • Drive collaboration across cross-functional teams to ensure consistent execution.
  • Provide leadership and operational oversight to project teams.

Skills

Site management leadership
Sponsor-facing liaison
Monitoring oversight
Cross-functional collaboration

Education

Bachelor's or Nursing degree

Job description

Worldwide Clinical Trials is seeking a Senior Clinical Trial Manager to lead site management across the full trial lifecycle, partnering with sponsors, CRAs, and cross-functional project teams to ensure high-quality outcomes. This is a remote role in the United States with travel up to 25%.

You will oversee monitoring activities, drive collaboration, and guide teams to successful study execution in a patient-focused, compliant environment.

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