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Pharmacovigilance Metrics Governance Senior Professional

Novo Nordisk
4+ years
INR 12 LPA – 18 LPA
Bangalore, India
1 June 16, 2026
Job Description
Job Type: Full Time Education: M.Pharm/B.Pharm or M.Sc. Skills: Communication Skills, CPC Certified, CPT, Data Analysis, Document Management, Life Science, Regulatory Compliance, Waterfall Model, GCP guidelines

Pharmacovigilance Metrics Governance Senior Professional

Location: Bangalore, Karnataka, India
Employment Type: Full-Time
Company: Novo Nordisk

Position Summary

The Pharmacovigilance Metrics Governance Senior Professional is responsible for supporting the governance, monitoring, reporting, and continuous improvement of global Pharmacovigilance (PV) quality and compliance metrics across Global Patient Safety (GPS). The role focuses on strengthening PV system oversight through governance frameworks, digital tools, compliance monitoring, quality metrics management, inspection readiness, and stakeholder collaboration to ensure patient safety and regulatory compliance globally.

Key Responsibilities

PV Metrics Governance & Compliance Monitoring

  • Support implementation and maintenance of the Global PV Metrics Governance Framework.

  • Monitor pharmacovigilance quality and compliance metrics across Global Patient Safety functions.

  • Ensure adherence to global pharmacovigilance regulations, quality standards, and internal requirements.

  • Support governance processes that strengthen oversight of the global PV system.

Quality & Compliance Reporting

  • Operationalize and coordinate PV governance meetings.

  • Prepare quality and compliance reports, dashboards, and performance metrics.

  • Support escalation and tracking of quality and compliance issues.

  • Ensure timely reporting of key pharmacovigilance performance indicators.

Process Improvement & Digital Transformation

  • Drive continuous improvement initiatives related to PV quality systems.

  • Support enhancement of digital tools, dashboards, and reporting processes.

  • Contribute to automation and optimization projects within Global Patient Safety.

  • Align PV monitoring processes with corporate Quality Management Review requirements.

Stakeholder Management

  • Collaborate with Global Patient Safety teams, affiliates, quality teams, and business stakeholders.

  • Partner with internal and external stakeholders to harmonize PV processes.

  • Benchmark PV quality and compliance practices against industry standards.

  • Facilitate cross-functional collaboration across headquarters and regional teams.

Audit, Inspection & CAPA Management

  • Support regulatory inspections, audits, and inspection readiness activities.

  • Facilitate Corrective and Preventive Action (CAPA) activities.

  • Track audit observations and compliance improvement initiatives.

  • Ensure effective closure of quality and compliance findings.

Training & Knowledge Management

  • Deliver internal and external training programs related to PV quality and compliance.

  • Promote knowledge sharing and continuous improvement culture.

  • Support development of best practices across Global Patient Safety functions.

  • Mentor and guide stakeholders on governance and compliance processes.

Educational Qualification

  • Bachelor's Degree in Life Sciences, Pharmacy, Biotechnology, Clinical Research, Healthcare, or related discipline.

Experience Required

  • Minimum 4+ years of Pharmacovigilance experience.

  • Experience in PV Operations, Drug Safety, or Pharmacovigilance Quality & Compliance.

  • Strong understanding of global pharmacovigilance regulations and requirements.

  • Experience supporting regulatory inspections and audits.

  • Experience working with PV systems, databases, and compliance monitoring processes.