Global Study Asset Manager

Clearline Recruitment Ltd

Welwyn Garden City

Hybrid

GBP 88,000 - 98,000

Full time

8 days ago
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Benefits offered by this job

25 days holiday plus Bank Holidays
Hybrid working with home working Flex
Minimum 2-3 days per week in the офис

Job summary

Clearline Recruitment Ltd is assisting a leading global healthcare organisation in recruiting a Global Study Asset Manager. The role is based in Welwyn Garden City, offering hybrid working with 2–3 days in the office and a 6-month contract inside IR35.

You will oversee the operational delivery of a portfolio of global clinical studies, engage with CROs, vendors and cross‑functional teams, and ensure study plans align with ICH-GCP and regulatory requirements.

Qualifications

  • Significant clinical study management experience within global trials.
  • Strong knowledge of ICH-GCP and drug development process.
  • Experience overseeing CROs, vendors and cross-functional stakeholders.
  • Ability to manage study timelines, quality, risks and KPIs.
  • Experience leading operations from planning to database lock.
  • Comfort operating in a fast-paced global environment.

Responsibilities

  • Coordinate 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.

Skills

Global study management
Global clinical trials
ICH-GCP knowledge
CRO/vendor oversight
Study delivery
Stakeholder management

Education

Life Sciences degree
Equivalent experience

Job description

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
The Requirements
  • 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
The Role
  • 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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