Job Description

Your new company

Are you an experienced Pharmacovigilance professional looking to make a significant impact within a global, research-driven pharmaceutical organisation?

We are partnering with a leading international biopharmaceutical company to recruit an Associate Director Pharmacovigilance on a 12-month contract basis. This is an excellent opportunity for a safety science expert to contribute to the development and lifecycle management of innovative medicines while influencing patient safety strategy at a global level.

Working within a highly collaborative safety organisation, you will provide strategic pharmacovigilance leadership across both clinical development and post-marketing activities, supporting benefit-risk decision-making and ensuring the highest standards of patient safety.

Your new role

As Associate Director Pharmacovigilance, you will play a key role within multidisciplinary global teams, providing expert safety oversight across a diverse product portfolio.

Key responsibilities include:

Providing pharmacovigilance and safety science expertise throughout the product lifecycle, from early development through to marketed products.

Serving as a core member of product safety and study teams, providing strategic safety input and oversight.

Leading signal detection, signal evaluation, and signal management activities.

Conducting benefit-risk assessments and supporting key safety governance decisions.

Managing post-marketing safety activities and contributing to safety strategy development.

Authoring, reviewing, and overseeing aggregate safety reports, including: DSURs, PBRERs / PSURs. Safety assessment reports, Regulatory safety responses.

Providing oversight of individual and aggregate case reporting activities.

Supporting development and maintenance of: Company Core Data Sheets (CCDS), Investigator's Brochures (IB), Risk Management Plans (RMPs), REMS documentationProduct labelling and safety communications

Contributing safety expertise to clinical development programmes and cross-functional project teams.

Supporting health authority interactions relating to safety and risk management.Influencing product safety strategy and contributing to broader clinical development objectives.

What you'll need to succeed

We are keen to hear from experienced Pharmacovigilance professionals with a strong background in safety science within the pharmaceutical, biotechnology, or CRO sector.

You will ideally possess:

PhD, MSc, PharmD, Medical Degree, or other postgraduate qualification in a Life Sciences or healthcare-related discipline.

Significant pharmacovigilance and drug safety experience.

Strong expertise in signal detection, signal management, benefit-risk evaluation, and risk management.

Proven experience authoring and reviewing DSURs, PBRERs, PSURs, and other aggregate reports.

A thorough understanding of global PV regulations, ICH guidelines, GVP, and GxP requirements.

Knowledge of the end-to-end clinical trial lifecycle and post-marketing safety processes.

Experience working within global cross-functional and matrix environments.Excellent analytical skills with the ability to interpret and communicate complex scientific and safety data.

Strong stakeholder management and presentation skills.

The ability to work independently, take ownership, and drive safety initiatives with minimal supervision.

Experience supporting both development and marketed products within a global pharmaceutical environment.

What you need to do now

This is a fantastic opportunity to join a world-class organisation at the forefront of healthcare innovation, working on cutting-edge therapies and contributing directly to patient safety on a global scale.

If you're looking for a high-impact contract role where your safety science expertise will influence key development and post-marketing decisions, we'd love to hear from you.

Click 'apply now' to forward an up-to-date copy of your CV, or call Roberta Atkins on (phone number removed)

Before you apply for this position, it is vital that you are in possession of a UK passport or relevant visa to work without restrictions in the UK and must be based in the UK