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, collaborative team environment, and impactful work.
- Other info: Opportunity to lead projects and improve processes in a dynamic setting.
- Why this job: Make a difference in patient safety while developing your career.
- Qualifications: Degree in health or life sciences; extensive pharmacovigilance experience preferred.
The predicted salary is between 50000 - 65000 € 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.
Benefits
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 in London 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 foster a culture of collaboration and continuous professional development, offering you the chance to lead impactful projects while working alongside dedicated colleagues. With a commitment to employee growth and a focus on meaningful contributions, our company stands out as an exceptional employer in the pharmaceutical industry.
StudySmarter Expert Advice🤫
We think this is how you could land Senior Pharmacovigilance Specialist in London
✨Tip Number 1
Network like a pro! Reach out to your connections in the pharmaceutical industry, especially those in pharmacovigilance. Attend industry events or webinars to meet potential employers and get your name out there.
✨Tip Number 2
Prepare for interviews by brushing up on your knowledge of UK and EU PV regulations. Be ready to discuss how your experience aligns with the responsibilities of the Senior Pharmacovigilance Specialist role. We want you to shine!
✨Tip Number 3
Showcase your skills! Create a portfolio that highlights your previous work in pharmacovigilance, including any audits or compliance projects you've managed. This will give you an edge when discussing your qualifications.
✨Tip Number 4
Don’t forget to apply through our website! It’s the best way to ensure your application gets noticed. Plus, we love seeing candidates who are proactive about their job search.
We think you need these skills to ace Senior Pharmacovigilance Specialist in London
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 emphasise your communication and stakeholder management skills. We want to see how you’ve successfully collaborated across functions and driven improvements in your previous roles.
Apply Through Our Website:For the best chance of success, make sure to apply through our website. This way, we can easily track your application and ensure it gets the attention it deserves!
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 Communication Skills
As a Senior Pharmacovigilance Specialist, you'll need to communicate effectively with various stakeholders. Prepare to share examples of how you've successfully managed relationships or influenced decisions in past roles. This will highlight your stakeholder management skills.
✨Be Ready for Scenario Questions
Expect questions that put you in hypothetical situations related to audits, inspections, or compliance issues. Think through how you would handle these scenarios in advance, focusing on your strategic mindset and attention to quality.
✨Demonstrate Your Organisational Skills
With responsibilities like managing local PV documents and aggregate reports, it’s crucial to show that you can prioritise and organise effectively. Bring examples of how you’ve successfully managed multiple projects or tasks simultaneously in your previous roles.
