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Discover International

Clinical Trial Manager

United Kingdom
Posted about 19 hours ago
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Discover International is partnered with a UK-based CRO is seeking a Clinical Trial Manager to lead the operational delivery of Phase I–IV clinical trials for pharmaceutical and biotech sponsors, managing cross-functional teams and study timelines from start-up through close-out.

Key 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

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I’m in my final year doing Economics and I don’t know whether to apply for grad schemes now or do a masters first. What do you think?

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Also worth knowing: most autumn 2026 applications are open now. Timing matters more than you think.

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Graduate Consultant — 2026 Scheme

PwC·London, UK
£35,000/yr

Why you're a good match

Strong

Your economics background and your summer at a regional bank line up with what PwC looks for on the consulting scheme. Applications close in four weeks.

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Why you're a good match

You’ve got the grades and the economics background, and your bank internship is exactly the experience this scheme looks for. Apply soon — deadlines close within the month.

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Experience fit

Your summer at the bank plus your econometrics coursework map directly to the day-one responsibilities on this scheme — client modelling, market briefings, and deal support.

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Skills & Experience

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  • Life sciences degree (or equivalent experience)
  • 4+ years in clinical trial management within a CRO, pharma, or biotech setting
  • Proven line management/mentoring experience
  • Strong knowledge of ICH-GCP, UK/EU trial regulations, and risk-based monitoring
  • Experience managing study budgets and vendors
  • Experience in oncology, rare disease, or cardiovascular trials
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Skills

Clinical Trial Management
Line Management
ICH-GCP
Budget Management
Vendor Oversight
Site Monitoring
Risk-Based Monitoring
Study Start-up
Feasibility Assessments
Inspection Readiness
Oncology
Rare Disease
Cardiovascular Trials
MHRA Regulations
UK/EU Trial Regulations
Cross-functional Team Leadership

Location

United Kingdom

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