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Senior Clinical Trial Manager

ICON · Blue Bell +2 more

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Clinical OperationsFull-timeCompany career page

The apply link worked recently (not employer-confirmed).

Role summary

ICON seeks a Senior Clinical Trial Manager to oversee clinical trial operations from initiation through closeout across diverse studies. The role requires leading cross-functional teams, ensuring regulatory compliance, managing budgets and timelines, and driving successful study outcomes in a remote capacity.

Where this listing comes from

This listing was compiled by RoleLantern from the employer's publicly available posting on Workday, captured and rephrased by RoleLantern using automated (AI) tools on 2026-10-04 (originally posted 2026-10-04). It was not submitted or confirmed by the employer through RoleLantern. Details may be inaccurate, incomplete, outdated, or no longer available; please confirm with the employer's official posting before applying.

What they're looking for

  • Bachelor's degree in Life Sciences, Health Sciences, Nursing, Pharmacy, or equivalent education and experience
  • Significant clinical trial management experience in CRO, pharmaceutical, or biotechnology setting
  • Strong understanding of clinical trial operations, ICH-GCP guidelines, and regulatory requirements
  • Demonstrated success leading clinical studies from start-up through database lock
  • Experience managing study timelines, budgets, vendors, and cross-functional stakeholders
  • Proven ability to identify risks and solve complex operational challenges
  • Ability to travel up to 20% as needed

What you'll be doing

  • Lead operational delivery of assigned clinical trials, ensuring timelines, budgets, quality standards, and milestones are met
  • Drive study start-up activities, site activation, enrollment strategies, and execution through database lock
  • Develop and implement study oversight plans, monitoring strategies, and risk mitigation approaches
  • Provide oversight of study progress, monitoring activities, clinical metrics, and site performance
  • Mentor Clinical Research Associates and cross-functional team members while ensuring ICH-GCP and regulatory compliance
CompensationCompetitive base salary and performance-related incentives

Privacy & handoff

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What RoleLantern checked

RoleLantern compiled this listing from the employer's public posting. We check that the application link is live and how recently the role appeared — the employer has not submitted or confirmed it on RoleLantern.

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RoleLantern checkedNeeds clarity

“RoleLantern checked active” means only that the application link was working when we last checked, on the date shown. It is not a guarantee that the role, employer, or any statement in the posting is accurate, current, lawful, or legitimate.

Date posted1 day ago
Last source checkToday
Salary listedNeeds clarity
Location clearClear
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