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BioTalent

Medical Lead Contractor

United Kingdom
Posted about 14 hours ago
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Medical Lead Consultant

Remote | UK or Europe
6 Month Contract | Full Time

BioTalent is exclusively supporting a global biopharmaceutical organisation that is seeking an experienced Medical Lead Consultant to provide medical oversight across both Clinical Development and Pharmacovigilance/Safety activities.

This is a highly visible role offering the opportunity to influence programmes across the full product lifecycle, working on innovative biologic and biosimilar products spanning multiple therapeutic areas.

The successful consultant will work closely with cross functional stakeholders across Clinical Development, Drug Safety, Regulatory Affairs, and Pharmacovigilance, providing strategic and operational medical leadership.

The Opportunity

This position combines post marketing safety responsibilities with hands on clinical development support and medical monitoring activities. A significant focus will be supporting ongoing pharmacovigilance initiatives, including the implementation and optimisation of modern safety systems, while also providing medical oversight for global clinical development programmes.

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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?

Honest answer — it depends on where you want to end up. A lot of top grad schemes (Big 4, civil service, banking) don’t need a masters. Let’s look at the ones you’d be competitive for now, and we can decide if a masters actually adds anything.

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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Key Responsibilities

  • Provide medical leadership and expertise across the full product lifecycle
  • Act as medical reviewer for Individual Case Safety Reports (ICSRs)
  • Lead and contribute to signal detection, signal evaluation, aggregate safety reports, and benefit-risk assessments
  • Partner closely with Pharmacovigilance teams to ensure robust patient safety oversight
  • Serve as Medical Monitor for clinical studies, including outsourced CRO managed trials
  • Review and interpret clinical data to support programme decision making
  • Contribute to the preparation and review of clinical trial documentation
  • Support scientific publications and medical communications activities
  • Provide medical input into regulatory authority interactions where required
  • Ensure compliance with GCP and GVP requirements
  • Collaborate with global Clinical Development teams and external stakeholders

Ideal Background

  • Medical degree (MD or equivalent)
  • Strong experience within Clinical Development and/or Pharmacovigilance
  • Prior experience serving as a Medical Monitor or Medical Lead within clinical trials
  • Expertise reviewing safety data, ICSRs, aggregate reports, signal detection, and benefit-risk evaluations
  • Experience supporting biologics, biosimilars, or complex pharmaceutical products is highly desirable
  • Strong understanding of GCP and GVP regulations
  • Ability to work effectively within global, cross functional teams
  • Consultancy or contractor experience is advantageous

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Contract Details

  • Remote working across the UK or Europe
  • Full time engagement
  • Initial 6 month contract
  • Strong likelihood of extension
  • Immediate interview process
  • Two stage interview process consisting of an initial screening discussion followed by a panel interview

Interested?

As the exclusive recruitment partner for this engagement, we are conducting an active search on behalf of our client and arranging interviews immediately.

If you have experience spanning Clinical Development, Medical Monitoring, Drug Safety, or Pharmacovigilance and would like to learn more, please send your CV along with your availability for a confidential discussion.

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Skills

Medical Oversight
Clinical Development
Pharmacovigilance
Medical Monitoring
Signal Detection
Benefit-Risk Assessment
ICSR Review
GCP Compliance
GVP Compliance
Regulatory Affairs
Biologics
Biosimilars
Clinical Trial Documentation
Medical Communications
Strategic Leadership
Cross-functional Collaboration

Location

United Kingdom

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