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Pv Veeva Manager (Pharmacovigilance Veeva Vault Manager)

Tcs
TCS
5-12 years
preferred by company
Mumbai, India
1 May 13, 2026
Job Description
Job Type: Full Time Education: B.Pharm/M.Pharm/M.Sc.or equivalent in life sciences Skills: Medical Terminology, mRS and EQ-5D-5L., Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs

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

Location: Mumbai, Maharashtra, India
Job Type: Full-Time
Experience Required: 5–12 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 Veeva Manager to lead pharmacovigilance technology operations, safety system governance, and drug safety process optimization within a fast-paced life sciences environment. This role is ideal for professionals with strong expertise in pharmacovigilance operations, Veeva Vault Safety administration, regulatory compliance, and safety data management.

The ideal candidate will oversee the implementation, maintenance, customization, and strategic optimization of the Veeva Vault Safety platform, ensuring seamless adverse event reporting, safety data integrity, regulatory compliance, and cross-functional operational excellence.

This opportunity is well suited for senior pharmacovigilance professionals with experience in drug safety systems, global reporting requirements, and healthcare technology transformation.

Key Responsibilities

Veeva Vault Safety System Management

  • Lead end-to-end administration, operation, maintenance, and optimization of the Veeva Vault Safety platform.
  • Configure, customize, and enhance system functionalities to align with organizational workflows and regulatory requirements.
  • Monitor system performance, troubleshoot operational issues, and coordinate upgrades, enhancements, and user support activities.
  • Ensure optimal system utilization across pharmacovigilance and drug safety operations.

Pharmacovigilance Operations & Safety Workflow Management

  • Manage workflows for adverse event case processing, safety surveillance, risk management, signal monitoring, and regulatory reporting activities.
  • Support safety operations aligned with global pharmacovigilance standards and internal compliance frameworks.
  • Collaborate with pharmacovigilance teams to improve operational efficiency, case management quality, and reporting timelines.
  • Support process standardization and automation initiatives within drug safety operations.

Regulatory Compliance & Safety Reporting

  • Ensure full compliance with global pharmacovigilance regulations including FDA, EMA, ICH guidelines, and applicable international reporting standards.
  • Support preparation, review, and submission of periodic safety reports and required regulatory safety documentation.
  • Stay informed about changing pharmacovigilance regulations and implement necessary system or workflow updates.
  • Support audit readiness, inspection preparation, and compliance governance activities.

Safety Data Management & Analytics

  • Oversee collection, validation, processing, and management of pharmacovigilance safety data.
  • Ensure integrity, security, confidentiality, and accuracy of adverse event and safety-related information.
  • Generate safety reports, dashboards, and analytical insights for internal teams, leadership, and regulatory stakeholders.
  • Support data-driven risk assessment and pharmacovigilance decision-making.

Cross-Functional Collaboration

  • Partner closely with clinical operations, regulatory affairs, medical safety, IT, quality assurance, and compliance teams.
  • Participate in cross-functional governance meetings to discuss safety trends, risk mitigation, and operational improvements.
  • Align Veeva Vault Safety capabilities with broader drug development and safety monitoring objectives.

Process Improvement & Strategic Optimization

  • Identify opportunities to improve pharmacovigilance workflows, reporting efficiency, and system performance.
  • Support digital transformation initiatives related to drug safety systems and healthcare technology modernization.
  • Contribute to best practice development, SOP optimization, and pharmacovigilance process excellence initiatives.

Required Qualifications

  • Bachelor’s or Master’s degree in Pharmacy, Life Sciences, Nursing, Biomedical Sciences, or a related healthcare discipline.
  • Master of Pharmacy (M.Pharm) preferred.
  • 5–12 years of relevant experience in pharmacovigilance, drug safety operations, safety systems management, or life sciences technology roles.
  • Hands-on expertise with Veeva Vault Safety is strongly preferred; experience with similar pharmacovigilance safety systems is also valuable.
  • Strong understanding of global pharmacovigilance regulations, safety reporting obligations, and compliance standards.
  • Experience in adverse event case processing, safety reporting, risk management, and pharmacovigilance workflows.
  • Strong analytical, troubleshooting, data management, and problem-solving capabilities.
  • Excellent communication, collaboration, and stakeholder management skills.
  • Ability to work independently and within cross-functional team environments.