Pharmacovigilance and Scientific Information Manager

RBW Consulting; Woking; Hybrid; GBP 85,000 - 110,000; Full time

Job summary

RBW Consulting is seeking a Pharmacovigilance and Scientific Information Manager for our client in Woking, with an option for up to 2 days remote per week. You will lead PV and SI strategy, oversee UK PV operations, and mentor a small team.

You will ensure UK regulatory compliance (GxP) and collaborate with global PV and Medical Affairs teams to align local activities with global initiatives. A life sciences degree and 5–10 years PV experience are required.

Qualifications

• Life science degree or Health Professional qualification.
• 5–10 years of pharmacovigilance experience.
• Proven leadership and line-management experience.
• Strong understanding of UK PV regulations, GxP and industry best practices.

Responsibilities

• Lead development and implementation of PV and SI strategies, processes and platforms.
• Act as UK National Contact Person for PV with MHRA oversight.
• Mentor and manage PV/SI staff, ensuring timely processing of safety information.
• Ensure PV/SI processes are audit-ready and compliant with GxP.
• Collaborate with Global PV and Medical Affairs teams to support global initiatives.

Skills

PV expertise

Leadership

Regulatory knowledge

Communication

Education

Life science degree or Health Professional qualification

Job description

Pharmacovigilance and Scientific Information Manager

Location: Woking (option for up to 2 days per week remote work)

A leading global manufacturer of pharmaceutical products across the UK and Europe, is seeking an experienced and dynamic Pharmacovigilance (PV) and Scientific Information (SI) Manager to join their Scientific Affairs team and lead the way in ensuring the highest standards of safety and information management.

Your Impactful Role

As the PV and SI Manager, you will be at the heart of commitment to safety and excellence. You will:

• Lead Strategy Development: Drive the development and implementation of PV and SI strategies, processes, and platforms, ensuring that they align with both UK legislation and the business' global standards.
• Act as the UK National Contact Person for PV: Serve as the primary liaison with the MHRA, maintaining oversight of all UK PV cases, ensuring compliance, and leading the UK pharmacovigilance system master file (PSMF).
• Manage and Mentor: Oversee a team of professionals, providing leadership, mentorship, and guidance, while managing resources to ensure the accurate and timely processing of safety information.
• Ensure Compliance and Quality: Maintain and improve PV and SI processes, ensuring they are always audit-ready and compliant with GxP standards.
• Collaborate Globally: Work closely with our Global Pharmacovigilance and Medical Affairs teams to ensure that local activities support and enhance global initiatives.

What You'll Bring:

• Expertise: A life science degree or qualification as a Health Professional, with 5-10 years of experience in pharmacovigilance.
• Leadership Skills: Previous line management experience and the ability to inspire and develop your team.
• Regulatory Knowledge: A thorough understanding of UK PV regulations, GvP, and industry best practices.
• Communication Skills: The ability to represent the company with external stakeholders, including the MHRA, healthcare professionals, and industry bodies.