Quick Summary
Key Responsibilities
Oversee protocol execution, timelines,
Technical Tools
OtherResearch Manager
Responsibilities
~1 min read- →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
~1 min read- 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.
Location & Eligibility
Where is the job
Maidenhead, United Kingdom
On-site at the office
Who can apply
GB
Listing Details
- Posted
- September 29, 2026
- First seen
- September 29, 2026
- Last seen
- September 29, 2026
Posting Health
- Days active
- 0
- Repost count
- 0
- Trust Level
- 54%
- Scored at
- September 29, 2026
Signal breakdown
freshnesssource trustcontent trustemployer trust
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