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Barrington James

Interim Director of Pharmacovigilance

London
Posted about 15 hours ago
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Contract | Freelance/Interim | Remote (EU/UK) | Immediate start | Full-time

A growing biopharmaceutical company is seeking an experienced Interim Director of Pharmacovigilance to provide senior drug-safety leadership during a period of transition and growth. This is a contract engagement suited to a hands-on PV leader who can step in at pace, hold the function together, and leave it stronger, whether bridging to a permanent hire or standing up capability ahead of a key milestone.

The role

Reporting into senior management, you'll take ownership of the end-to-end pharmacovigilance system and act as the senior point of accountability for safety across the portfolio. You'll balance strategic oversight with genuine hands-on delivery in a lean, fast-moving environment.

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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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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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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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Key Responsibilities

  • Provide leadership and oversight of the global PV system, ensuring ongoing GVP compliance and audit/inspection readiness.
  • Support or deputise for the QPPV, including PSMF maintenance and safety governance.
  • Oversee signal detection, benefit-risk evaluation and risk-management activities across the portfolio.
  • Own delivery of aggregate safety reports (PSUR/PBRER, DSUR) and regulatory safety commitments.
  • Manage CRO/vendor safety relationships and safety-data-exchange agreements (SDEAs).
  • Lead and mentor a small PV team, and interface with Regulatory, Clinical, Quality and Medical.
  • Drive inspection readiness and CAPA management ahead of regulatory milestones.

What We're Looking For

  • Substantial pharmacovigilance experience (typically 10+ years), including at MAH or biotech level, with time at Director or equivalent.
  • Strong working knowledge of EU GVP and global PV regulatory requirements.
  • EU QPPV experience or eligibility highly desirable.
  • Demonstrable experience standing up, scaling or turning around a PV function.
  • Track record of regulatory inspections and audit readiness.
  • Life sciences, pharmacy or medical background.
  • Available immediately or at short notice on a contract basis.

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Details

Fully remote (EU/UK-based). Competitive rate, dependent on experience. Initial 6 month contract with scope to extend.

Interested, or know someone who fits? Get in touch with Ollie Thorpe at Barrington James for a confidential conversation.

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Skills

Pharmacovigilance
GVP Compliance
Signal Detection
Benefit-Risk Evaluation
Risk Management
Aggregate Safety Reporting
PSUR/PBRER
DSUR
Vendor Management
SDEA
Audit Readiness
CAPA Management
QPPV
PSMF Maintenance
Regulatory Compliance
Leadership

Location

London, England, United Kingdom

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