Manager – PV Global Safety Database, Pharmacovigilance, Epidemiology & Risk Management
Location: Noida, India | Job ID: R2516332 | Category: Consulting | Employment Type: Full-Time
About Cencora
Cencora is a global leader in healthcare and life sciences, committed to creating healthier futures for people and animals worldwide. Our teams drive innovation, patient safety, and operational excellence in pharmacovigilance and risk management. Join our collaborative environment to make an impact in global drug safety and medical information management.
Position Overview
Cencora is seeking a Manager for PV Global Safety Database to oversee the administration, configuration, and compliance of pharmacovigilance (PV) and medical information databases. The role ensures regulatory compliance, database integrity, and effective support to internal and client-facing PV operations.
Key Responsibilities
Configure, maintain, and optimize global safety and medical information databases.
Manage user accounts, roles, access controls, and security permissions.
Perform routine system checks, troubleshooting, and maintenance in collaboration with IT and vendor teams.
Support system implementations, post-go-live activities, and database migration projects.
Assist in creating and executing validation documentation (URS, FRS, IQ/OQ/PQ) in compliance with GxP and 21 CFR Part 11.
Provide first-level support for database-related issues via internal helpdesk.
Develop and update user training materials, conduct training sessions, and onboard new users.
Collaborate with cross-functional teams to implement system upgrades and new features.
Analyze complex business needs, recommend solutions, and ensure alignment with pharmacovigilance workflows and regulatory requirements.
Prepare for and support internal and external audits and inspections.
Qualifications & Experience
Education: Bachelor’s degree in Life Sciences, Computer Science, or a related field.
Experience: Minimum 2+ years in PV safety database administration, pharmacovigilance systems, or handling medical information inquiries.
Strong understanding of PV workflows, regulatory requirements, and GxP compliance.
Experience with validation documentation, SaaS/cloud-hosted PV systems, and medical information systems preferred.
Excellent organizational, communication, and problem-solving skills.
Ability to work independently, manage priorities, and collaborate effectively with global teams.
Why Join Cencora
Lead and maintain critical global safety databases supporting pharmacovigilance and risk management operations.
Collaborate with cross-functional teams to implement cutting-edge PV and medical information technology solutions.
Participate in audits, inspections, and compliance initiatives for global regulatory standards.
Access career growth opportunities in a globally recognized healthcare organization.
Equal Employment Opportunity
Cencora is committed to equal employment opportunity regardless of race, color, religion, sex, sexual orientation, gender identity, genetic information, national origin, age, disability, veteran status, or any other legally protected class. Reasonable accommodations are provided during the recruitment process.
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