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Pv Manager Veeva

Tcs
TCS
5-12 years
₹18 LPA – ₹30 LPA
Mumbai, India
10 March 16, 2026
Job Description
Job Type: Full Time Education: M.Pharm Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

PV Manager – Veeva Vault Safety

Company: (Pharmacovigilance / Drug Safety Services Organization)
Location: Mumbai
Job Type: Full-Time
Experience: 8 – 12 Years (Pharmacovigilance / Drug Safety Systems)
Qualification: Master of Pharmacy (M.Pharm) / Bachelor’s or Master’s in Pharmacy, Nursing, Life Sciences
Apply By: 12 June 2026
Approx Salary: ₹18 LPA – ₹30 LPA


Job Overview

The PV Manager – Veeva Vault Safety role focuses on managing pharmacovigilance systems and drug safety processes using Veeva Vault Safety.

The position is responsible for overseeing adverse event reporting workflows, safety data management, regulatory compliance, and system configuration to support global pharmacovigilance activities.

The candidate will collaborate with clinical, regulatory, and IT teams to ensure effective safety data monitoring and compliance with international pharmacovigilance regulations.


Key Responsibilities

1. Veeva Vault Safety System Management

  • Oversee operation and maintenance of Veeva Vault Safety.

  • Configure and customize system workflows according to organizational and regulatory requirements.

  • Implement workflows for adverse event reporting, safety signal monitoring, and risk management.


2. Pharmacovigilance Compliance

  • Ensure system compliance with global pharmacovigilance regulations including:

    • U.S. Food and Drug Administration

    • European Medicines Agency

    • International Council for Harmonisation guidelines

  • Prepare and submit periodic safety reports and regulatory documents.


3. Safety Data Management

  • Manage collection, processing, and analysis of safety data.

  • Develop safety reports and dashboards for internal teams and regulatory authorities.

  • Ensure data integrity, confidentiality, and regulatory compliance.


4. Cross-Functional Collaboration

  • Work closely with clinical development, regulatory affairs, and IT teams.

  • Support integration of pharmacovigilance processes with the drug development lifecycle.

  • Participate in cross-functional safety meetings to evaluate safety signals and risk trends.


5. Process Improvement

  • Monitor regulatory changes and implement system updates and workflow improvements.

  • Identify opportunities to improve pharmacovigilance operations and data management efficiency.

  • Contribute to continuous improvement initiatives within PV systems and processes.


Required Skills

Technical Skills

  • Extensive experience with Veeva Vault Safety or similar PV systems

  • Strong knowledge of global pharmacovigilance regulations and reporting requirements

  • Expertise in safety data management and regulatory reporting

Professional Skills

  • Strong analytical and problem-solving abilities

  • Excellent communication and stakeholder management skills

  • Ability to work independently and in cross-functional teams


Key Competencies

  • Pharmacovigilance system management

  • Drug safety data analysis and reporting

  • Regulatory compliance and safety monitoring

  • Cross-functional collaboration in drug development

  • Continuous improvement of PV processes