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Pharmacovigilance Metrics Governance Principal Specialist

Novo Nordisk
6+ years
INR 10 LPA – 15 LPA
Bangalore, India
1 June 12, 2026
Job Description
Job Type: Full Time Education: M.Pharm/B.Pharm or M.Sc. Skills: MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, mRS and EQ-5D-5L., Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Pharmacovigilance Metrics Governance Principal Specialist
Company: Novo Nordisk
Location: Bangalore, Karnataka, India
Department: PV Quality & Compliance Monitoring, Global Patient Safety
Experience: 6+ Years

Overview

Novo Nordisk is hiring a Pharmacovigilance Metrics Governance Principal Specialist to support the governance framework for monitoring, measuring, and reporting global pharmacovigilance quality and compliance metrics. The role focuses on PV governance, compliance oversight, audit readiness, stakeholder management, and continuous improvement of the global PV system.

Key Responsibilities

PV Governance & Metrics

  • Support implementation and maintenance of global PV governance frameworks

  • Monitor and report PV quality and compliance metrics

  • Facilitate governance meetings and issue escalation processes

  • Support global oversight of pharmacovigilance system performance

Quality & Compliance

  • Ensure adherence to PV quality and compliance requirements

  • Support CAPA (Corrective and Preventive Action) activities

  • Drive inspection and audit readiness initiatives

  • Monitor compliance trends and recommend improvements

Process Improvement

  • Lead cross-functional quality improvement projects

  • Harmonize PV processes with internal and external standards

  • Benchmark processes against industry best practices

  • Improve operational efficiency while maintaining compliance

Stakeholder Management

  • Collaborate with Global Patient Safety teams, affiliates, and external partners

  • Build strong relationships across global functions

  • Support strategic discussions related to PV quality and compliance

Required Qualifications

Education

  • Bachelor's Degree in Life Sciences or related field

Experience

  • Minimum 6 years of Pharmacovigilance experience

  • Strong background in PV Operations, Compliance, or Quality

  • Experience supporting regulatory inspections and audits

  • Knowledge of global PV regulations and GxP requirements

Required Skills

  • Pharmacovigilance Operations

  • PV Quality & Compliance

  • GxP Compliance

  • CAPA Management

  • Audit & Inspection Readiness

  • Quality Management Systems

  • PV Metrics & KPI Management

  • Regulatory Compliance

  • Stakeholder Management

  • Risk Assessment

  • Process Improvement

  • Safety Databases & Systems

  • Data Analysis & Reporting