Barrington James
Interim Director of Pharmacovigilance

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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?
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
Why you're a good match
StrongYour 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.
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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No noise. No "maybe this fits." Just roles with a clear explanation of why they're right — and where to focus when applying.
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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