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Senior pharmacovigilance scientist

Welwyn Garden City
Clearline Recruitment Ltd
Scientist
Posted: 18h ago
Offer description

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 01273 063 769 between 8:30am - 5:00pm, Monday to Friday.

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