Senior Metabolic Clinical Trial Manager — Remote Leadership

Worldwide Clinical Trials

Clayton (NC)

Remote

USD 112,000 - 222,000

Full time

8 days ago

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Job summary

Worldwide Clinical Trials is seeking a Senior Clinical Trial Manager for a remote US role. You will lead clinical site management and monitoring activities across studies, partnering with sponsors, CRAs, and cross-functional teams to drive high-quality outcomes.

Responsibilities include directing site activities, ensuring budget adherence, and maintaining rigorous trial standards. Travel up to 25% is required, and a valid passport is necessary.

Qualifications

  • The candidate has a Bachelor’s Degree or Nursing Degree and 2+ years in Clinical Trial Manager or equivalent roles.
  • 4+ years as a Clinical Research Associate with metabolic or endocrinology trials.
  • Ability to travel up to 25% and hold a valid passport.
  • Proven ability to lead, motivate, and support remote teams.

Responsibilities

  • Lead clinical research associates and site management teams through full study lifecycle.
  • Serve as the primary sponsor-facing contact for monitoring and site activities.
  • Build strong partnerships and ensure clear communication during study execution.
  • Oversee monitoring deliverables to meet study objectives, quality, and budget.
  • Identify out-of-scope activities and communicate impacts and solutions.
  • Foster collaboration across cross-functional teams for consistent site management execution.
  • Provide leadership and operational oversight to project teams for high-quality conduct.

Skills

Clinical trial management
Remote team leadership
Study monitoring
Cross-functional collaboration

Education

Bachelor’s Degree or Nursing Degree

Job description

Worldwide Clinical Trials is seeking a Senior Clinical Trial Manager for a remote US role. You will lead clinical site management and monitoring activities across studies, partnering with sponsors, CRAs, and cross-functional teams to drive high-quality outcomes.

Responsibilities include directing site activities, ensuring budget adherence, and maintaining rigorous trial standards. Travel up to 25% is required, and a valid passport is necessary.

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