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Global Study Asset Manager
Remote / Online - Candidates ideally in
Welwyn Garden City, Hertfordshire, AL8, England, UK
Listed on 2026-10-10
Welwyn Garden City, Hertfordshire, AL8, England, UK
Listing for:
Clearline Recruitment Ltd
Full Time, Part Time, Remote/Work from Home
position Listed on 2026-10-10
Job specializations:
-
Business
Regulatory Compliance Specialist
Job Description & How to Apply Below
Role:
Global Study Asset Manager
Location:
Welwyn Garden City (Hybrid - 2/3 days in office)
Hours:
Full-time, 37.5 hours per week
Contract:
6 months, Inside IR35
Pay: £339.27 - £376.97 per day PAYE basic or £450 - £500 per day Umbrella
An excellent opportunity has arisen for a highly experienced Global Study Asset Manager to join one of our longstanding clients, a leading global healthcare organisation.
This is a senior clinical operations role responsible for the operational delivery of a portfolio of global clinical studies, working across internal study teams, CROs, vendors and cross-functional stakeholders.
Benefits- 25 days holiday plus Bank Holidays
- Hybrid working with home working flexibility
- Minimum 2-3 days per week in the office
- Free onsite parking
- Opportunity to work within a leading global healthcare organisation
- Exposure to complex, global clinical studies
- Significant clinical study management experience within global clinical trials
- Strong clinical operations and study delivery experience
- Phase III experience is essential
- Strong knowledge of the drug development process, ICH and GCP
- Experience managing studies from operational planning through to database lock
- Experience overseeing CROs, vendors and cross-functional stakeholders
- Strong understanding of study timelines, quality, risks and KPIs
- Life Sciences degree or equivalent experience preferred
- Confident operating in a fast-paced, complex global environment
- Coordinate the operational delivery of multiple studies within an asset portfolio
- Ensure studies progress in line with ICH-GCP, SOPs and study plans
- Support development of key study documents and operational plans
- Manage study recruitment expectations and forecasting
- Oversee study performance, quality, timelines, risks and KPIs
- Partner closely with CROs and internal global study teams
- Lead third-party vendor selection, set-up, oversight and close-out
- Maintain inspection readiness
- Manage IMP supply and shipment where required
- Drive operational improvements and efficiencies across studies
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