Job Title: Pharmacovigilance Agreements Specialist
Location: Mumbai, India
Experience Required: 3–7 Years
Job Function: Business Process Services – Executive Level
Tata Consultancy Services (TCS) is a leading global IT and consulting organization, recognized for delivering innovative solutions across multiple industries. Within the life sciences domain, TCS supports pharmaceutical clients in ensuring compliance, operational excellence, and patient safety. We are seeking a skilled Pharmacovigilance Agreements Specialist to join our Mumbai team and manage global and local pharmacovigilance contractual arrangements.
The Pharmacovigilance Agreements (PVA) Specialist is responsible for managing the lifecycle of PVAs, ensuring compliance with company standards and global pharmacovigilance regulations. The role involves drafting, reviewing, updating, and maintaining agreements, as well as ensuring effective communication and collaboration with internal and external stakeholders.
This role is ideal for candidates with experience in pharmacovigilance regulations, contract management, and global pharmaceutical operations.
Draft, revise, and review Global and Local Pharmacovigilance Agreements (PVAs) to ensure alignment with company requirements
Address internal and external stakeholder comments and ensure timely finalization of PVAs
Manage dedicated PVA mailbox, including queries and correspondence
Announce new or revised PVAs to relevant client stakeholders
Maintain and update a centralized PVA tracker for all active agreements, including reconciliations and status updates
Monitor compliance of active PVAs and prepare dashboards/reports as required
Support Project Managers and team leads in maintaining project-related documents and trackers
Upload and organize all PVA documentation in the company repository
Participate in team meetings, providing operational updates and highlighting any issues or escalations
Ensure adherence to global regulatory standards including ICH guidelines and Good Pharmacovigilance Practices (GVP)
Educational Background:
Bachelor of Pharmacy (B.Pharm) / Master of Pharmacy (M.Pharm)
Bachelor of Science (B.Sc) / Master of Science (M.Sc) in Life Sciences or related fields
Experience:
3–7 years of relevant experience in pharmacovigilance agreements, contract management, or regulatory operations
Strong working knowledge of global pharmacovigilance regulations, including ICH guidelines and GVP modules
Skills & Competencies:
Expertise in drafting and reviewing contractual PVAs
Excellent attention to detail, organizational, and documentation skills
Strong communication skills for cross-functional and client interactions
Ability to manage multiple agreements and ensure timely compliance
Proficiency in MS Office, dashboards, and document management systems
Work with a global leader in technology and life sciences solutions
Opportunity to specialize in pharmacovigilance contracts across global and local markets
Collaborative environment supporting professional growth and skill development
Exposure to cross-functional teams, client engagements, and compliance best practices
Apply Now to be part of a dynamic team where your expertise in pharmacovigilance agreements will directly impact patient safety and regulatory compliance across global markets.
Application Deadline: 13-Apr-2026
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