Pharmacovigilance Agreements Specialist

Roles & Responsibilities
•Draft new and revised Pharmacovigilance Agreements (PVAs) as per company and regulatory requirements
•Review PVAs to ensure quality, accuracy, and global pharmacovigilance compliance
•Address internal and collaborating company comments on PVAs
•Manage and monitor the dedicated PVA mailbox
•Announce new and revised PVAs to relevant stakeholders
•Maintain and update global PVA trackers and reconciliations
•Perform compliance monitoring of effective PVAs and prepare dashboards
•Support Project Managers in maintaining project documents and trackers
•Upload, archive, and maintain PVAs in the company repository
•Participate in team meetings and provide regular status updates

Qualifications
•B.Pharm, M.Pharm, B.Sc, M.Sc

Experience

•Minimum 3-7 years of hands-on experience in Pharmacovigilance

• •Prior experience in drafting and managing Global and Local Pharmacovigilance Agreements
  
  Skills
  •Strong knowledge of ICH & GVP regulations
  •PVA drafting and management
  •Life sciences domain expertise
  •Documentation skills
  •Stakeholder coordination
  •Good communication skills
  
  About the Compnay
  Tata Consultancy Services (TCS) is a global leader in IT services, consulting, and business solutions, headquartered in India and part of the Tata Group. With operations in over 50 countries, TCS serves clients across industries including life sciences, healthcare, pharmaceuticals, banking, and manufacturing. The company is known for its strong focus on innovation, digital transformation, regulatory-compliant solutions, and employee development, delivering high-quality services that help organizations improve efficiency, compliance, and business performance worldwide.