At a Glance
- Tasks: Lead a team to ensure patient safety and compliance in pharmacovigilance.
- Company: Join Sanofi, an innovative biopharma company transforming lives with cutting-edge science.
- Benefits: Hybrid work model, competitive salary, and opportunities for professional growth.
- Other info: Be part of a diverse team driving breakthroughs in drug discovery.
- Why this job: Make a real impact on global health by improving drug safety and development.
- Qualifications: Healthcare professional or life sciences degree with pharmacovigilance experience.
The predicted salary is between 60000 - 75000 £ per year.
Location: Reading, UK
Job Type: Regular, Full-Time
Working Arrangements: Hybrid - 3 days per week on‑site in Reading and 2 days remote
About the job
As a Pharmacovigilance Manager, you'll lead a dedicated team to ensure the accurate and timely processing of all safety information while maintaining robust processes, compliance standards, training programs, and systems aligned with current legislation and company procedures. In this critical role, you'll be responsible for delivering an efficient multi country pharmacovigilance organization that upholds the highest standards of patient safety and regulatory excellence.
Main responsibilities
- Lead local patient safety operations - Manage and oversee the team to ensure accurate and timely processing of all PV activities including individual/aggregate reporting, SUSAR management, local signal detection, safety agreements, literature monitoring, and risk management activities.
- Ensure regulatory compliance - Maintain all pharmacovigilance processes and training in full alignment with regulations and global company policies, keeping operations inspection and audit-ready at all times.
- Support clinical and commercial programs - Provide effective PV support for clinical studies, post-authorization studies, patient support programmes, digital initiatives, and market research activities.
- Manage quality and documentation - Maintain all quality documentation within the Pharmacovigilance department, ensuring timely resolution of corrective/preventative actions and appropriate escalation procedures.
- Drive team development and performance - Recruit, manage, and motivate direct reports; provide training, coaching, and development opportunities while ensuring adherence to HR procedures and fostering a motivated, engaged team environment.
- Oversee vendor relationships - Ensure effective day-to-day vendor management, contractual compliance, and performance against agreed targets while adhering to company procurement processes.
- Facilitate cross-functional collaboration - Foster accurate, timely communication and effective collaboration between Business Unit functions across local and global Sanofi entities and Pharmacovigilance departments.
- Maintain professional expertise - Stay current with Good Pharmacovigilance Practice, UK/EU legislation, and industry best practices while demonstrating personal leadership in ethics, governance, and safety standards.
About you
- Qualified Healthcare Professional (Pharmacist, Nurse, Dentist or Pharmacy Technician) OR degree in Life Sciences.
- In-depth knowledge of UK/EU pharmacovigilance requirements and strong understanding of Good Pharmacovigilance Practice (GVP).
- Significant experience in pharmacovigilance audit/inspection, signal detection, and risk management.
- Proven line management experience with ability to motivate, coach, and develop high-performing teams.
- Excellent stakeholder management and communication skills, with ability to collaborate effectively across cross‑functional and global teams.
Why choose us?
- Be part of a pioneering biopharma company that engages patients early in drug development and uses their insights to design studies that reflect real‑world needs.
- Work at the forefront of drug discovery, harnessing cutting‑edge AI, data, and digital platforms to push the boundaries of science.
- Help improve the lives of millions of people globally by making drug development quicker and more effective.
- Enjoy opportunities to collaborate beyond your area of expertise, working with diverse teams across science, clinical, and digital fields to spark new ideas and drive breakthroughs.
We are proud to be a Disability Confident Employer, committed to offering interviews to candidates who request consideration under the Scheme and meet the minimum requirements for this role. If you have a disability and require adjustments for the interview process, please email us at diversity.recruitmentUKIE@sanofi.com. We are dedicated to ensuring an inclusive and supportive experience for all applicants.
Pharmacovigilance Manager in Reading employer: Meeveem Limited
Sanofi is an exceptional employer located in Reading, UK, offering a hybrid work model that promotes a healthy work-life balance. As a pioneering biopharma company, we provide our employees with opportunities for professional growth and development while fostering a collaborative and inclusive work culture. Join us to be at the forefront of drug discovery, where your contributions will directly impact patient safety and improve lives globally.
StudySmarter Expert Advice🤫
We think this is how you could land Pharmacovigilance Manager in Reading
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We think you need these skills to ace Pharmacovigilance Manager in Reading
Some tips for your application 🫡
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How to prepare for a job interview at Meeveem Limited
✨Understand the Science
Make sure you brush up on key pharmaceutical concepts and recent developments in the industry. You might get asked some technical questions during the interview at Meeveem Limited that show your grasp of drug development processes or regulatory requirements, so be ready to discuss them clearly.
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In a full-time pharmaceutical role, understanding the regulatory landscape is crucial. Prepare for situational questions that may test your problem-solving skills concerning compliance and safety standards. You could be asked how you'd handle a hypothetical issue regarding a drug’s market release, so think through your approach.
