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Manager, Pv Global Safety Database, Pharmacovigilance Epidemiology & Risk Management

Cencora
Cencora
2+ years
Not Disclosed
10 Dec. 30, 2025
Job Description
Job Type: Full Time Education: B.Sc/M.Sc/M.Pharma/B.Pharma/Life Sciences 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

Manager – PV Global Safety Database

Pharmacovigilance, Epidemiology & Risk Management

Location: Noida, India
Employment Type: Full-Time
Category: Consulting
Posted Date: October 28, 2025
Job ID: R2516332
Affiliated Entity: PharmaLex India Private Limited (A Cencora Company)


About Cencora

Cencora is a global healthcare services organization focused on improving patient outcomes and advancing public health through science-driven, compliant, and technology-enabled solutions. Our teams work across the pharmaceutical, biotechnology, and life sciences landscape to ensure patient safety, regulatory excellence, and operational efficiency. At Cencora, every role contributes directly to our mission of creating healthier futures worldwide.


Role Overview

Cencora is seeking a Manager – PV Global Safety Database to support global pharmacovigilance and medical information technology operations. This role is responsible for the configuration, administration, validation, and ongoing maintenance of safety and medical information databases used across global PV programs.

The ideal candidate will possess strong technical expertise in pharmacovigilance systems, a solid understanding of regulatory compliance, and the ability to manage stakeholder expectations across internal teams and external clients.


Key Responsibilities

  • Configure, administer, and maintain global safety and medical information databases supporting pharmacovigilance operations.

  • Manage user accounts, system roles, and access controls in accordance with data integrity and security requirements.

  • Perform routine system health checks, maintenance activities, and issue monitoring.

  • Provide system support during implementation, upgrades, and post-go-live phases.

  • Act as first-level support for database-related issues through internal helpdesk platforms.

  • Troubleshoot and resolve technical issues in collaboration with IT teams and external vendors.

  • Support the preparation, execution, and maintenance of validation documentation including URS, FRS, and IQ/OQ/PQ.

  • Ensure ongoing compliance with GxP, 21 CFR Part 11, data integrity principles, and global regulatory requirements.

  • Develop, update, and maintain training materials for safety system end-users.

  • Conduct system training sessions and onboarding programs for new users.

  • Support internal initiatives and client-facing projects related to PV and Medical Information technology platforms.

  • Collaborate with cross-functional stakeholders to implement system enhancements, upgrades, and new functionalities.

  • Analyze complex business and client requirements and recommend scalable technical solutions.

  • Support database migration activities, system transitions, and data reconciliation efforts.

  • Participate in and support internal and external audits and regulatory inspections.


Required Qualifications

  • Bachelor’s degree in Life Sciences, Computer Science, Pharmacy, or a related discipline.

  • Formal training or certification in pharmacovigilance systems or GxP compliance is an advantage.


Experience Requirements

  • Minimum 2+ years of hands-on experience in safety database administration and/or pharmacovigilance or medical information systems.

  • Demonstrated experience supporting PV workflows, regulatory reporting, and safety data management.

  • Practical exposure to system validation, change management, and compliance documentation.


Key Skills and Competencies

  • Strong understanding of pharmacovigilance processes, global regulations, and safety system architecture.

  • Experience with medical information and safety databases used in pharmaceutical environments.

  • Familiarity with cloud-based PV systems and SaaS platforms.

  • High attention to detail with strong documentation and organizational skills.

  • Excellent communication and stakeholder management abilities.

  • Proactive, self-driven approach with strong problem-solving capabilities.

  • Ability to work independently as well as within cross-functional global teams.


What Cencora Offers

Cencora provides a professional and inclusive work environment with exposure to global pharmacovigilance programs and advanced safety technologies. Compensation and benefits are aligned with local market practices and may vary based on location and employment terms.


Equal Employment Opportunity

Cencora is an equal opportunity employer and is committed to maintaining a diverse and inclusive workplace. Employment decisions are made without discrimination based on race, color, religion, sex, sexual orientation, gender identity, genetic information, national origin, age, disability, veteran status, or any other protected characteristic.

Reasonable accommodations are provided to qualified individuals with disabilities in accordance with applicable legal requirements.