Talentmark are recruiting for an Associate Director, Drug Safety to join a company in the pharmaceutical industry on a contract basis for 12 months.

Salary:
-67.96 - -75.51 per hour PAYE or -90 - -100 per hour Umbrella/Ltd.

Associate Director, Drug Safety Role:

• Provide safety oversight and input across the full study lifecycle, from early development through to post-market.
• Lead post-market safety work, including signal evaluation, benefit-risk assessment and risk management.
• Own case reporting, including aggregate reports such as DSUR and PBRER.
• Drive signal detection and contribute to the strategic review of safety reports.
• Prepare and maintain risk management documents, including CCDS, labelling documents, RMPs and REMS.

Your Background:

• Strong understanding of GxP, regulated processes and the clinical trial lifecycle.
• Confident communicator, able to work with remote teams across different countries.
• Skilled in data analysis and statistical methods, with the ability to present findings clearly.
• Strong presenter, able to summarise key points for different audiences.
• Able to work independently with minimal supervision.
• A postgraduate qualification in a life sciences field (PhD, MSc, medical or PharmD) is preferred but not essential.

Company:
Our client is one of the world''s premier innovative biopharmaceutical companies, discovering, developing and providing products to help improve the lives of millions of people in the UK and around the world every year.

Location:
This role is based at our client''s site in Welwyn, 2 days per week in the office.

Apply
For more information, or to apply for this Associate Director, Drug Safety role please contact the Key Accounts Team on (phone number removed) or email (url removed). Please quote reference (Apply online only).

It is essential that applicants hold entitlement to work in the UK.

Please note: This role may be subject to a satisfactory basic Disclosure and Barring Service (DBS) check.