Lead Clinical Trial Manager – Global Phase I–IV Delivery

Discover International

Norwich

On-site

GBP 65,000 - 85,000

Full time

14 days+
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Job summary

Discover International seeks a Clinical Trial Manager in the UK to lead end-to-end delivery of Phase I–IV trials for pharmaceutical and biotech sponsors. You will manage cross-functional teams and timelines from start-up through close-out in a fast-paced CRO setting.

The role requires a life sciences degree and 4+ years in trial management, with experience in oncology, rare disease, or cardiovascular trials, and strong knowledge of ICH-GCP and trial regulations.

Qualifications

  • 4+ years in clinical trial management within a CRO, pharma, or biotech setting.
  • Life sciences degree or equivalent experience.
  • Strong knowledge of ICH-GCP, UK/EU trial regulations, and risk-based monitoring.
  • Experience in oncology, rare disease, or cardiovascular trials.

Responsibilities

  • Own end-to-end trial management for assigned studies, ensuring delivery on time, on budget, and to quality standards.
  • Line-manage CRAs/CRCs, overseeing site monitoring plans and performance.
  • Serve as primary point of contact for sponsors, providing status updates and risk escalation.
  • Develop and manage study budgets, timelines, and vendor/CRO oversight plans.
  • Ensure inspection readiness and compliance with ICH-GCP, MHRA, and sponsor SOPs.
  • Lead site selection, feasibility assessments, and study start-up activities.
  • Chair internal and sponsor study team meetings.

Skills

Line management
Mentoring

Education

Life sciences degree

Job description

Discover International seeks a Clinical Trial Manager in the UK to lead end-to-end delivery of Phase I–IV trials for pharmaceutical and biotech sponsors. You will manage cross-functional teams and timelines from start-up through close-out in a fast-paced CRO setting.

The role requires a life sciences degree and 4+ years in trial management, with experience in oncology, rare disease, or cardiovascular trials, and strong knowledge of ICH-GCP and trial regulations.

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