PV Product Lead – Pharmacovigilance & Data Governance

MSD; Rahway (NJ); Hybrid; GBP 106,000 - 167,000; Full time

Job summary

MSD is seeking a Product Manager for PV Reporting and Surveillance within its Information Technology group in the United States. The role leads pharmacovigilance strategies, ensuring patient safety and regulatory compliance across PV systems.

You will partner with Clinical, Regulatory, Safety, and Business Technology teams to manage roadmaps and implement PV/QC enhancements, driving milestones and stakeholder alignment in a fast-paced, regulated environment.

Qualifications

• Bachelor’s degree required.
• 6+ years in data governance, compliance, privacy, risk or related roles.
• Strong communication for technical and non-technical audiences.
• Experience with data governance, data products, digital solutions, and AI-enabled programs.
• Ability to develop policies, standards, SOPs, and governance processes.
• Knowledge of data management practices: data quality, metadata, security/privacy, master data management.

Responsibilities

• Partner with cross-functional teams to develop PV strategies meeting regulatory requirements.
• Manage and prioritize product backlog and align with objectives.
• Develop, maintain, and execute Product Strategy and Roadmap.
• Oversee PV systems, including adverse event reporting, case management, signal detection.
• Ensure PV processes adhere to regulatory requirements including ICH guidelines.
• Collaborate with Clinical, Regulatory, Safety to integrate PV into product development.

Skills

Data governance

Compliance

Privacy

Risk management

AI governance

Policy development

SOPs

Data management

Stakeholder management

Communication

Education

Bachelor’s degree

Master’s degree (preferred)

Tools

Veeva

Job description

MSD is seeking a Product Manager for PV Reporting and Surveillance within its Information Technology group in the United States. The role leads pharmacovigilance strategies, ensuring patient safety and regulatory compliance across PV systems.

You will partner with Clinical, Regulatory, Safety, and Business Technology teams to manage roadmaps and implement PV/QC enhancements, driving milestones and stakeholder alignment in a fast-paced, regulated environment.