Maidenhead
Posted: Sep 29, 2026
On-siteFull-time
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Job Description

Location: London (Hybrid) - 2–3 days/week on-site

We’re looking for an experienced Clinical Research Manager to lead country-level clinical trial operations. You’ll ensure performance, quality, and compliance across assigned protocols, manage vendors and sites, and collaborate with internal teams (PV, Regulatory, GMA, GHH). This is a customer-facing role with significant impact on trial delivery and country commitments.

Key Responsibilities:

  • Oversee protocol execution, timelines, and budgets
  • Ensure compliance with ICH-GCP and local regulations
  • Lead quality oversight and training for CRAs/CTCs
  • Build strong relationships with investigators and vendors
  • Contribute to local and regional strategy

Requirements:

  • 6–8 years’ clinical research experience (pharma/CRO/healthcare)
  • Strong knowledge of ICH-GCP and drug development
  • Excellent communication and leadership skills
  • Ability to manage multiple protocols and stakeholders
  • London-based, on-site 2–3 days/week

Apply now and make an impact on the future of clinical development!

Learn more about our EEO & Accommodations request here.

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Additional Info
Min. Experience
-
Job Location Type
On-site
Job Type
Full-time
Predicted Seniority Level
-
Job Duration
-
Language(s)
-
Est. Budget/Pay Rate
To be discussed
Est. hrs
-
Optimal Job Start
-
Job Industry
-
Job Function
-
Employer
Fortrea
Preferred Applicant Countries
Global
Job Ref
J267392D00820
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