Welcome Back

Google icon Sign in with Google
OR
I agree to abide by Pharmadaily Terms of Service and its Privacy Policy

Create Account

Google icon Sign up with Google
OR
By signing up, you agree to our Terms of Service and Privacy Policy
Instagram
youtube
Facebook

Regional Pharmacovigilance Senior Manager

Pharmiweb
pharmiweb
5-12 years
Not Disclosed
United Kingdom, England
10 March 24, 2026
Job Description
Job Type: Full Time Remote Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Regional Pharmacovigilance Senior Manager

Location: United Kingdom (Remote / Home-based)
Job Type: Full-Time
Experience Required: 7–12 years (minimum 5 years in Pharmacovigilance)

Overview
ICON Strategic Solutions is seeking an experienced Regional Pharmacovigilance Senior Manager to lead and oversee pharmacovigilance operations across global regions. This leadership role is critical in ensuring regulatory compliance, optimizing safety systems, and driving continuous improvement in drug safety processes. You will act as a key scientific and operational expert, collaborating with cross-functional teams and global stakeholders to enhance patient safety and regulatory excellence.

Key Responsibilities
Serve as a regional pharmacovigilance subject matter expert, providing scientific and regulatory guidance to internal and external stakeholders
Oversee pharmacovigilance activities to ensure compliance with global and local regulatory requirements, including GVP guidelines
Assess, develop, and harmonize pharmacovigilance processes across regions to align with client and regulatory standards
Support EU/UK QPPV and Regional PV Leads in maintaining and enhancing regional pharmacovigilance systems
Contribute to the development, maintenance, and updates of Pharmacovigilance System Master File (PSMF)
Collaborate with global teams including regulatory, medical, quality, legal, and commercial functions
Drive audit and inspection readiness activities, ensuring compliance with global safety standards
Monitor evolving safety regulations and provide strategic insights for implementation
Support innovation initiatives to improve efficiency and effectiveness of pharmacovigilance operations
Lead continuous improvement initiatives and contribute to KPI development and performance tracking
Build strong relationships with global affiliates and partners across multiple regions

Required Skills and Competencies
Strong expertise in pharmacovigilance regulations, GVP guidelines, and drug safety processes
In-depth understanding of drug development lifecycle and GxP compliance requirements
Proven experience in managing PSMF and safety systems
Excellent leadership, stakeholder management, and cross-functional collaboration skills
Strong analytical, problem-solving, and decision-making abilities
Effective communication and presentation skills with the ability to simplify complex information
Ability to work independently in a global, matrixed environment
Proficiency in Microsoft Office and safety-related systems

Eligibility Criteria
Master’s degree in Pharmacy, Life Sciences, Nursing, or a related field (PharmD/MD preferred)
7–12 years of experience in the pharmaceutical, biotechnology, CRO, or regulatory environment
Minimum 5 years of hands-on experience in pharmacovigilance or drug safety

Preferred Qualifications
Experience working with global regulatory authorities and international pharmacovigilance systems
Prior involvement in audits, inspections, and regulatory submissions
Exposure to multi-regional pharmacovigilance operations and compliance frameworks

About the Company
ICON Strategic Solutions is a global leader in healthcare intelligence and clinical research services. The organization partners with pharmaceutical, biotechnology, and medical device companies to accelerate clinical development and deliver innovative healthcare solutions worldwide.

Why Apply
Opportunity to lead global pharmacovigilance strategies and operations
Exposure to international regulatory frameworks and multi-regional safety systems
Leadership role with high visibility and cross-functional impact
Competitive compensation and comprehensive benefits package

Work Environment
This is a remote, home-based role based in the United Kingdom, with flexibility to travel for client meetings, audits, and inspections as required.