CareerPlan

Associate Director, Technical Product Management

USA - New Jersey - RahwayFull-time$142k–$224k2026-10-29 → 2026-11-10

Core

Lead the development and implementation of pharmacovigilance (PV) strategies, processes, and systems to ensure regulatory compliance and patient safety in a pharmaceutical R&D environment.

Role type

Senior IC Product Manager (Pharmacovigilance & Data Governance)

Builds

Pharmacovigilance software platforms, data governance frameworks, and compliance systems for adverse event reporting and signal detection.

Domain

Life Sciences / Healthcare / Regulatory Compliance

Required skills

Pharmacovigilance strategy, Data governance, Regulatory compliance (ICH), Stakeholder management, Product roadmap planning, System architecture, Quality control, Signal detection, Master data management, Agile/Lean development

Preferred skills

MBA, Privacy and data protection, Quality management systems, Healthcare/Life sciences experience, Veeva platform

Technologies

Veeva, Agentic AI-enabled programs

Responsibilities

Partner with cross-functional teams to develop PV strategies meeting regulatory requirements; Manage and prioritize the product backlog; Develop and execute Product Strategy and Roadmap; Oversee PV systems for adverse event reporting and case management; Ensure compliance with global PV regulations and ICH guidelines; Collaborate with Clinical, Regulatory, and Safety teams to integrate PV processes; Partner with Business Technology teams for system implementation.

Seniority

Senior, hands-on IC