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.
Top Skills
What We Do
Fortrea (Nasdaq: FTRE) is a leading global provider of clinical development and patient access solutions to the life sciences industry. We partner with emerging and large biopharmaceutical, medical device and diagnostic companies to drive healthcare innovation that accelerates life changing therapies to patients in need. Fortrea provides phase I-IV clinical trial management, clinical pharmacology, differentiated technology-enabled trial solutions and post-approval services. Fortrea’s solutions leverage three decades of experience spanning more than 20 therapeutic areas, a passion for scientific rigor, exceptional insights and a strong investigator site network.
Our talented and diverse team working in more than 90 countries is scaled to deliver focused and agile solutions to customers globally. Learn more about how Fortrea is becoming a transformative force from pipeline to patient at Fortrea.com.
