Role: Senior Pharmacovigilance Scientist

Location: Welwyn (Hybrid working - 2 days per week in the office)

Hours: Full-time

Pay: £33.98 - £37.76 (PAYE) per hour or £45.00 - £50.00 (UMB/LTD) per hour

Contract: 12-month contract (Outside IR35)

An excellent opportunity has arisen for a Senior Pharmacovigilance Scientist to join one of our longstanding clients, a leading organisation within the pharmaceutical and healthcare sector.

This role sits within a Patient Safety Operations function, supporting the compliant processing, reporting, oversight, and quality of safety data and individual case safety reports.

Benefits:

• 12-month contract opportunity
• Hybrid working with 2 days onsite per week
• Opportunity to work within a specialist pharmacovigilance function
• Exposure to global safety operations, audits, and regulatory processes

The Requirements:

• Strong pharmacovigilance experience, particularly within ICSR processing and oversight
• Experience supporting quality, compliance, audits, and inspections
• Proven ability to lead complex projects and manage multiple stakeholders
• Experience with vendor oversight and service provider management
• Strong pharmacovigilance systems knowledge and ability to support process improvements
• Good understanding of international safety regulations, including ICH, EU GVP, and FDA
• Excellent communication, stakeholder management, and problem-solving skills
• Medical device expertise desirable
• Degree-level education or equivalent practical pharmacovigilance experience

The Role:

• Overseeing service providers delivering ICSR and safety reporting activities
• Acting as a subject matter expert for internal and external stakeholders
• Supporting compliant safety data processing, reporting, and quality oversight
• Leading complex initiatives and process improvement projects
• Preparing for and supporting audits, inspections, and regulatory queries
• Identifying root causes of non-compliance and supporting CAPA activity
• Assessing the impact of new or updated regulatory requirements
• Maintaining high-quality documentation, training, and procedural standards
• Supporting risk escalation and ensuring issues are managed appropriately

If you're an experienced pharmacovigilance professional looking for a specialist contract opportunity, please apply to this Senior Pharmacovigilance Scientist role or contact Chloe McCausland at Clearline Recruitment on between 8:30am - 5:00pm, Monday to Friday.