Senior Pharmacovigilance Specialist at Merck

Job Description:

Senior Pharmacovigilance (PV) Specialist

We’re seeking a hands-on Senior PV Specialist to join our UK & Ireland country operations team. You’ll take ownership of local PV activities, keep us compliant, and be a trusted partner to local business teams. On a day-to-day basis you’ll support the management of local initiatives and data sources, assist with audits and inspections, maintain PV systems and documentation, and oversee ARMM and RMP activities.

This role suits someone who is organised, proactive and enjoys working across functions and with global PV stakeholders. In a challenging, fast‑moving environment you’ll make a direct impact, solve complex problems and grow your PV expertise.

What you’ll do:

• Execute local PV processes and ensure compliance with local legislation and global procedures (AE case handling, aggregate reports, patient programmes, local PV agreements).

• Support the management of adverse event intake, triage, follow-up and submissions.

• Support PV audits, inspections and self-inspections; contribute to development and closure of CAPAs.

• Maintain local PV documents, training materials and local training resources; support onboarding of new colleagues.

• Support aggregate report operations; scheduling, coordinating and maintaining timely submission of aggregate safety reports

• Implement local Risk Management Plans (RMPs) and associated risk-minimisation activities.

• Implement and oversee Risk Minimisation Measures and Additional Risk Minimisation Measures.

• Monitor Health Authority communications and advise stakeholders; represent PV in cross-functional meetings.

• Review local initiatives (marketing, patient programmes, digital tools) for PV compliance.

• Support business continuity plans and participate in projects that improve PV processes.

What we need from you:

Education:

• Degree in health, life sciences or medical sciences, or equivalent experience.

Experience:

• Extensive PV experience in the pharmaceutical industry preferred (or equivalent experience).

• Strong knowledge of AE reporting, UK and EU PV regulations and PV quality systems.

• Experience with PV audits or Health Authority inspections preferred.

Key skills

• Fluent in English (written and spoken).

• Excellent communication and stakeholder-management skills.

• Strong organisation, prioritisation and project-management abilities.

• Comfortable working independently and collaborating across functions.

• Effective negotiation and influencing skills; able to drive improvements.

• Strategic mindset with a strong attention to quality and regulatory compliance.

Desirable

• Previous experience in the UK Pharmacovigilance environment

• Experience with ARMM and RMP activities

Why join us:

You will play a visible role in keeping patients safe and enabling our business teams to operate with confidence. We offer opportunities to lead projects, develop professionally and work with a collaborative, cross functional team.

Closing date for applications: 22/05/2026

Required Skills:

Compliance Monitoring, Cross-Functional Collaboration, Data Analysis, Drug Safety Surveillance, Patient Safety, Pharmaceutical Management, Pharmaceutical Regulatory Compliance, Pharmacovigilance, Regulatory Compliance, Regulatory Reporting, Risk Management, Safety Procedures, Stakeholder Management

Preferred Skills:

Current Employees apply HERE

Current Contingent Workers apply HERE

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Employee Status:

Regular

Relocation: VISA Sponsorship:Travel Requirements:

Flexible Work Arrangements:

Hybrid

Shift: Valid Driving License:Hazardous Material(s):

Job Posting End Date:

05/23/2026

**A job posting is effective until 11:59:59PM on the day BEFORE the listed job posting end date. Please ensure you apply to a job posting no later than the day BEFORE the job posting end date.