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RWE Study Manager

United Kingdom
Posted about 17 hours ago
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Job Title: RWE Study Manager (Phase IV Studies)

Location: Remote (UK)
Employment Type: Full-time, Permanent

We're partnering with a leading global pharmaceutical organization to find an experienced RWE Study Manager to lead the delivery of Phase IV and Real-World Evidence (RWE) studies across multiple countries.

This is a fantastic opportunity to take ownership of multinational evidence-generation studies, working closely with Medical Affairs, CROs, investigators, and external partners from study start-up through to final reporting.

What you'll be doing:

  • Lead the planning, execution, and delivery of Phase IV and RWE studies
  • Manage study timelines, budgets, resources, risks, and key milestones
  • Oversee CROs, vendors, sites, and external research partners throughout the study lifecycle
  • Ensure compliance with GCP, GPP, regulatory requirements, SOPs, and data privacy standards
  • Partner cross-functionally with Medical Affairs, Epidemiology, Biostatistics, Regulatory Affairs, Pharmacovigilance, Market Access, and Commercial teams

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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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What we're looking for:

  • Degree in Life Sciences, Epidemiology, Public Health, Pharmacy, or a related field
  • 4+ years of Study Management experience within clinical research or pharmaceutical settings
  • Experience managing Phase IV, observational, non-interventional, registry, or RWE studies internationally
  • Strong project management, stakeholder management, vendor oversight, and risk management capabilities
  • Knowledge of real-world data, post-marketing research methodologies, and pharmacovigilance requirements

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Why this opportunity?

  • Lead high-impact studies that contribute to evidence generation and patient outcomes
  • Work within a highly collaborative and cross-functional global environment
  • Gain exposure to scientific publications, congress presentations, and medical strategy initiatives
  • Take ownership of complex multinational studies from start-up to final reporting
  • Fully remote position with flexibility and autonomy

Interested or know someone who could be a fit? Feel free to reach out directly or apply confidentially!

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Skills

Study Management
Project Management
Stakeholder Management
Vendor Oversight
Risk Management
Real-World Evidence
Phase IV Studies
Observational Studies
Non-Interventional Studies
Registry Studies
Pharmacovigilance
Medical Affairs
Epidemiology
Biostatistics
Regulatory Affairs
Market Access

Location

United Kingdom

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