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Barrington James

Interim Director of Pharmacovigilance

London
Posted 1 day ago
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Interim Pharmacovigilance Director — Remote, Europe

Contract

Remote (EU-based)
Competitive Hourly Rate
6-month initial engagement, likely to extend
Immediate start

A biotech is looking for a seasoned Pharmacovigilance Director to lead its safety function on an interim basis during a period of growth. A senior, hands-on leadership role owning the PV system end to end, interim cover, working ahead of a permanent appointment.

What You'll Be Doing

  • Leading the pharmacovigilance function and owning the PV system and its operating model
  • Acting as the senior point of accountability for the safety of the [marketed and/or development] portfolio
  • Overseeing signal management, benefit-risk and aggregate reporting to the required standard
  • Owning the PV System Master File, SDEAs and vendor/partner oversight
  • Driving inspection and audit readiness, and leading any CAPA through to closure
  • Interfacing with the QPPV office, regulators (EMA/national/MHRA) and cross-functional leadership
  • Providing safety leadership through [launch / M&A integration / affiliate build-out — delete as applicable]

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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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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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What We're Looking For

  • Extensive pharmacovigilance experience (7+ years), with a track record in senior PV leadership roles.
  • Proven ownership of a PV system across MAHs.
  • Strong command of EU GVP, the global regulatory framework and inspection expectations
  • Demonstrable experience of building, scaling or remediating a PV function
  • QPPV or Deputy QPPV experience [desirable]
  • Based in the EU/EEA and able to work remotely; fluent English

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Desirable

  • Experience in rare disease and oncology.
  • Track record leading through inspections and delivering CAPA's
  • Experience of M&A safety integration or interim leadership assignments.

What's On Offer

  • Senior day rate reflecting the accountability and seniority of the role
  • Fully remote, EU-wide
  • Real authority and ownership from day one
  • A quick, straightforward process

Freelance and interim only. If it's a fit, send your CV or current profile and I'll come back to you quickly. othorpe@barringtonjames.com

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Skills

Pharmacovigilance
PV System Ownership
Signal Management
Benefit-Risk Assessment
Aggregate Reporting
PV System Master File
SDEA
Vendor Oversight
Audit Readiness
CAPA
EU GVP
Regulatory Compliance
QPPV
Rare Disease
Oncology
M&A Integration

Location

London, England, United Kingdom

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