20.06.22

Director – Pharmacovigilance

Director – Pharmacovigilance

TMC Pharma Services delivers an impressive range of services across rare and orphan disease, stem and cell-based therapies, biologics, and immuno-oncology.

With a track record of success extending to more than 20 years, TMC Pharma has an enviable global customer base, partnering with small and large organisations from across the pharma, biotech, and device sectors.

On the back of their success, TMC Pharma is embarking on an exciting expansion plan that will allow them to develop their offering and customers base.

Based from their beautiful headquarters on the Elvetham Park Estate nr Hartley Wintney just off the M3, TMC are looking to add an experienced Director to their expanding Pharmacovigilance team.

The Director will play a keen role in the growth, development, and deliverables of the team.

Deputising for the Head of Pharmacovigilance where required, the successful appointment will provide support and input to the strategic Pharmacovigilance advice given to TMC clients and colleagues.

Working on challenging, multi-geography projects, the Director will work alongside in-house Pharmaceutical Physicians and Associates, defining and maintaining company standards for PV, both in clinical trials and with marketed products.

Having functioned as a UK QPPV, the Director will be a technical authority across an active case load, bringing a keen eye for detail and identify opportunities for improvement.

As a proven project leader, you will bring rigor, process, and structure to deliverables in line with customer expectations. The Director will proactively manage resources (internally & externally), timelines, and safety risk management.

We would expect applicants hold a relevant level of academic qualification in a related life sciences field or a recognised nursing qualification.  You will have undertaken a post graduate qualification or equivalent in pharmacovigilance.

With more than ten years’ experience in a Pharmacovigilance function in the Pharmaceutical Industry, you will bring demonstrable knowledge of GVP, relevant global legislation and expertise in case handling.

PV experience from within the CRO environment is preferred, with a strong service orientation.

As well as technical competence, you will bring strong commercial acumen, the ability to manage budgets and manage commercial change.

A brilliant communicator, you will forge incredibly close relationships with key customer contacts, building highly productive, collaborative partnerships that deliver outstanding results.

If you are looking to take a leadership role where you will make a tangible difference to patients, then contact us today for a confidential conversation or simply apply at apply@leadcandidate.com with a copy of your CV.

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