Role: Associate Director of Pharmacovigilance
Location: Welwyn Garden City / Hybrid (2 days per week in the office)
Hours: Full-time
Pay: £67.96 - £75.51 per hour (PAYE) or £90 - £100 per hour (LTD/UMB )
Contract: 12-month contract, outside IR35
An excellent opportunity has arisen for an Associate Director of Pharmacovigilance to join one of our longstanding global pharmaceutical clients. This senior-level role will provide scientific leadership across pharmacovigilance and safety science activities, supporting both clinical development and post-marketing products whilst contributing to global product safety strategy.
Benefits
- Hybrid working with 2 days per week in Welwyn Garden City
- 12-month contract outside IR35
- 25 days holiday + bank holidays
- On-site and free parking
- Opportunity to support global development and marketed products
- Exposure to strategic pharmacovigilance and safety science activities
- Senior-level role within a collaborative global team
The Requirements
- Degree in Life Sciences or a related scientific discipline
- Postgraduate qualification (MSc, PhD, PharmD, Medical qualification or equivalent) advantageous
- Significant pharmacovigilance and safety science experience within the pharmaceutical industry
- Strong understanding of GxP, regulated processes and the end-to-end clinical trial lifecycle
- Experience leading post-marketing safety activities and benefit-risk assessments
- Experience producing aggregate safety reports, including DSURs and PBRERs
- Knowledge of signal detection, safety risk management and regulatory requirements
- Excellent communication, presentation and stakeholder management skills
- Ability to work independently and manage multiple priorities within a global environment
The Role
- Provide pharmacovigilance and safety science support across development and marketed products
- Lead signal evaluation, signal detection and benefit-risk assessments
- Manage individual and aggregate case reporting activities, including DSURs and PBRERs
- Contribute to global product safety strategy across clinical development programmes
- Prepare and maintain CCDS, Investigator Brochures, Risk Management Plans and safety-related labelling documentation
- Provide safety oversight and input into study management activities
- Support safety risk management and regulatory submissions
- Present complex scientific data clearly to internal stakeholders and cross-functional teams
- Collaborate with global teams to support pharmacovigilance initiatives and strategic objectives
- Contribute to continuous improvements across pharmacovigilance processes and practices
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Associate Director of Pharmacovigilance in Welwyn Garden City employer: Clearline Recruitment Ltd
Clearline Recruitment Ltd is an excellent employer, offering a vibrant work culture in the heart of Brighton, where innovation meets customer service excellence. Employees benefit from flexible hybrid working arrangements, competitive pay, and opportunities for professional growth within a supportive team environment, making it an ideal place for those seeking meaningful and rewarding employment.
