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Pv Manager – Veeva

Tcs
TCS
8-10 years
preferred by company
Mumbai, India
1 May 13, 2026
Job Description
Job Type: Full Time Education: M.Pharm/B.Pharm or M.Sc. Skills: Medical Coding, Medical Terminology, mRS and EQ-5D-5L., Narrative Writing, Research & Development, Technical Skill

Job Title: PV Manager – Veeva (Pharmacovigilance Manager – Veeva Vault Safety)

Location: Mumbai, Maharashtra, India
Job Type: Full-Time
Experience Required: 8–10+ Years (Freshers are not eligible)
Industry: Pharmacovigilance / Drug Safety / Life Sciences / Pharmaceuticals / Healthcare Technology
Department: Business Process Services / Pharmacovigilance Operations

About the Role
We are seeking an experienced PV Manager – Veeva to lead pharmacovigilance technology operations, drug safety process governance, and safety system optimization within a regulated life sciences environment. This senior-level opportunity is ideal for professionals with extensive expertise in pharmacovigilance operations, Veeva Vault Safety administration, global safety compliance, and clinical safety data management.

The ideal candidate will oversee the strategic use, maintenance, configuration, and enhancement of the Veeva Vault Safety platform, ensuring seamless safety case processing, regulatory compliance, adverse event reporting, and cross-functional operational efficiency.

This role is well suited for experienced pharmacovigilance leaders seeking high-impact responsibilities in drug safety systems and healthcare technology transformation.

Key Responsibilities

Veeva Vault Safety Leadership & System Management

  • Lead end-to-end management, administration, maintenance, and optimization of the Veeva Vault Safety system.
  • Configure, customize, and enhance platform workflows based on business requirements and global regulatory obligations.
  • Monitor system performance, identify operational issues, and coordinate upgrades, maintenance activities, and enhancement initiatives.
  • Ensure efficient and scalable system usage across pharmacovigilance and safety operations teams.

Pharmacovigilance Operations & Safety Process Oversight

  • Manage pharmacovigilance workflows related to adverse event reporting, case management, risk management, signal review support, and safety monitoring.
  • Drive operational excellence across drug safety processes aligned with internal SOPs and compliance frameworks.
  • Support process standardization, automation, and workflow optimization for pharmacovigilance operations.
  • Collaborate with internal teams to improve reporting quality, case processing efficiency, and safety governance.

Regulatory Compliance & Safety Reporting

  • Ensure Veeva Vault Safety processes remain compliant with FDA, EMA, ICH guidelines, Good Pharmacovigilance Practices (GVP), and global drug safety regulations.
  • Support preparation, review, and submission of periodic safety reports and regulatory documentation as required.
  • Monitor evolving regulatory requirements and implement system/process updates to maintain compliance.
  • Support audit readiness, inspections, compliance reviews, and quality governance activities.

Safety Data Management & Reporting Analytics

  • Oversee the collection, validation, management, and analysis of pharmacovigilance safety data.
  • Ensure confidentiality, integrity, accuracy, and traceability of safety information.
  • Develop dashboards, analytical reports, and performance insights for internal stakeholders and leadership teams.
  • Support data-driven pharmacovigilance risk assessment and reporting decision-making.

Cross-Functional Collaboration & Stakeholder Management

  • Work closely with clinical operations, medical safety, regulatory affairs, IT, compliance, and quality teams.
  • Participate in governance meetings to review safety trends, risk indicators, compliance updates, and operational performance.
  • Align Veeva safety capabilities with broader drug development, regulatory, and business objectives.

Continuous Improvement & Strategic Innovation

  • Identify opportunities for pharmacovigilance process optimization and technology modernization.
  • Contribute to digital transformation initiatives within safety operations and healthcare technology ecosystems.
  • Support SOP enhancements, best practice implementation, and operational excellence initiatives.

Required Qualifications

  • Bachelor’s or Master’s degree in Pharmacy, Nursing, Life Sciences, Biomedical Sciences, or related healthcare disciplines.
  • Master of Pharmacy (M.Pharm) preferred.
  • 8–10+ years of relevant experience in pharmacovigilance, drug safety operations, clinical safety systems, or life sciences safety technology roles.
  • Extensive hands-on experience with Veeva Vault Safety or equivalent pharmacovigilance safety platforms.
  • Strong understanding of global pharmacovigilance regulations, adverse event reporting requirements, and drug safety compliance standards.
  • Experience in pharmacovigilance data analysis, safety reporting, risk management, and regulatory operations.
  • Excellent analytical thinking, troubleshooting, documentation, and stakeholder communication skills.
  • Ability to work independently while effectively collaborating with cross-functional teams.