At a Glance
- Tasks: Manage local pharmacovigilance activities and ensure compliance with regulations.
- Company: Join a leading pharmaceutical company focused on patient safety.
- Benefits: Professional development, project leadership opportunities, and a collaborative team environment.
- Other info: Be part of a dynamic team with a strong focus on quality and compliance.
- Why this job: Make a real difference in patient safety while advancing your career.
- Qualifications: Degree in health or life sciences and extensive pharmacovigilance experience.
The predicted salary is between 46000 - 52000 € per year.
We’re seeking a hands‑on Senior Pharmacovigilance 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.
Responsibilities
- 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.
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.
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.
Application Deadline
Closing date for applications: 22/05/2026
Senior Pharmacovigilance Specialist employer: MSD in the UK
As a Senior Pharmacovigilance Specialist in our UK & Ireland operations, you will thrive in a dynamic and supportive work environment that prioritises patient safety and regulatory compliance. We offer robust professional development opportunities, a collaborative culture, and the chance to lead impactful projects that contribute to the well-being of patients and the success of our business. Join us to be part of a team that values your expertise and fosters growth in a meaningful way.
StudySmarter Expert Advice🤫
We think this is how you could land Senior Pharmacovigilance Specialist
✨Tip Number 1
Network like a pro! Reach out to professionals in the pharmacovigilance field on LinkedIn or at industry events. We can’t stress enough how valuable personal connections can be in landing that dream job.
✨Tip Number 2
Prepare for interviews by brushing up on your knowledge of UK and EU PV regulations. We recommend practising common interview questions related to compliance and risk management, so you can showcase your expertise confidently.
✨Tip Number 3
Don’t just wait for job openings to pop up! Be proactive and reach out to companies you admire, even if they’re not advertising positions. A well-crafted email expressing your interest can open doors we didn’t even know existed.
✨Tip Number 4
Finally, apply through our website! It’s the best way to ensure your application gets seen by the right people. Plus, it shows you’re genuinely interested in being part of our team. Let’s get you that Senior Pharmacovigilance Specialist role!
We think you need these skills to ace Senior Pharmacovigilance Specialist
Some tips for your application 🫡
Tailor Your CV:Make sure your CV is tailored to the Senior Pharmacovigilance Specialist role. Highlight your relevant experience in PV processes, compliance, and any specific projects you've led that align with our needs.
Craft a Compelling Cover Letter:Your cover letter should tell us why you're the perfect fit for this role. Share your passion for pharmacovigilance and how your skills can help us keep patients safe while supporting our business teams.
Showcase Your Skills:Don’t forget to highlight your communication and stakeholder management skills. We want to see how you’ve effectively collaborated across functions and driven improvements in your previous roles.
Apply Through Our Website:We encourage you to apply through our website for a smoother application process. It’s the best way for us to receive your application and get to know you better!
How to prepare for a job interview at MSD in the UK
✨Know Your Pharmacovigilance Stuff
Make sure you brush up on your knowledge of adverse event reporting and UK/EU regulations. Being able to discuss specific examples from your experience will show that you’re not just familiar with the theory but have practical insights too.
✨Showcase Your Compliance Skills
Prepare to talk about how you've ensured compliance in previous roles. Think of specific situations where you managed audits or inspections, and be ready to explain how you handled any challenges that arose.
✨Communicate Like a Pro
Since this role involves a lot of stakeholder management, practice articulating your thoughts clearly. Use examples that demonstrate your excellent communication skills, especially in cross-functional settings.
✨Be Ready for Scenario Questions
Expect questions that put you in hypothetical situations related to risk management plans or adverse event handling. Prepare by thinking through how you would approach these scenarios, focusing on your strategic mindset and attention to quality.
