Pharmacovigilance Manager

Haybury; Greater London; Hybrid; GBP 60,000 - 80,000; Full time

Job summary

A leading global pharmaceutical organization is seeking a Pharmacovigilance Manager to oversee product safety and compliance. The role involves leading operations, developing policies, and mentoring junior staff. Candidates should have a strong background in pharmacovigilance and stakeholder management.

Benefits

Competitive salary and bonus package

Comprehensive benefits

Hybrid working model

Qualifications

• Strong experience in Pharmacovigilance Operations for the UK.
• Experience in managing stakeholders and health authorities.

Responsibilities

• Lead Pharmacovigilance Operations and ensure compliance.
• Develop local Pharmacovigilance policies and training programs.
• Review safety data and conduct benefit-risk assessments.

Skills

Stakeholder Management

Cross-Functional Collaboration

Project Management

Education

Degree in Pharmacy

Degree in Medical

Degree in Science

Tools

Safety Databases

QMS

Job description

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Team Lead, Executive Search & Interim at Haybury

We have partnered with a leading global pharmaceutical organisation who are seeking a Pharmacovigilance Manager to join their team. In this pivotal role, you’ll oversee the safety of their products, ensuring compliance with industry standards and regulations.

If you have a strong background in pharmacovigilance and want to take on a role that drives meaningful change, this is for you!

Responsibilities:

As PV Manager, you will:

• Lead Pharmacovigilance Operations, providing strategic oversight and ensuring execution of safety activities in full compliance with safety reporting regulations
• Develop and evolve local Pharmacovigilance policies, procedures, and training programs that drive excellence in safety operations and foster a culture of compliance
• Lead the review of safety data, signal detection, and benefit-risk assessments, ensuring timely and proactive safety decision-making
• Champion the integration of strategy for Patient Safety, as well as Pharmacovigilance across therapeutic areas, embedding safety intelligence into every phase of the product life cycle
• Build and maintain strong partnerships with regulatory authorities, external vendors, and cross-functional teams to ensure smooth collaboration and inspection readiness
• Stay ahead of the curve by monitoring regulatory developments and translating them into actionable updates for systems and practices
• Inspire and mentor junior team members, driving continuous improvement and contributing to the strength of the function

What You Bring to the Role:

• Degree in Pharmacy, Medical, or Science
• Strong experience in Pharmacovigilance Operations for the UK within Pharmaceutical Industry
• You excel at managing stakeholders, including suppliers and health authorities, and thrive in cross-functional collaborations
• You’re well-versed in safety databases, QMS, and audit/inspection support for pharmacovigilance processes
• You know how to prioritise, plan, and lead Pharmacovigilance-related projects in a regulated environment

In Return, you will receive:

• A competitive salary and bonus package
• Comprehensive benefits, including a hybrid working model
• The chance to shape the future of patient safety and pharmacovigilance, in a dynamic and global organisation

If you are ready to advance your career and have the skills and ambition for this position, please email your CV to Emma Nayani-James.

Keywords: Pharmacovigilance, PV, Patient Safety, PSPV, MHRA, Signal Detection, Regulations, Compliance, HPRA, Risk Management, PV Operations, Policy, Safety, Clinical Trials, Post Marketing, Drug Safety

Seniority level

• Seniority level

  Mid-Senior level

Employment type

• Employment type

  Full-time

Job function

• Job function

  Manufacturing, Project Management, and Research

• Industries

  Research Services, Pharmaceutical Manufacturing, and Biotechnology Research

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