Pharmacovigilance Agreements Specialist
Location: Mumbai, India
Experience Required: 3–7 Years
Application Deadline: 13 April 2026
Employment Type: Full-Time
Job Function: Business Process Services
Role Level: Executive
Job ID: 391019
Industry: Pharmacovigilance | Drug Safety | Life Sciences
Role Overview
We are hiring a Pharmacovigilance Agreements Specialist to support global pharmacovigilance operations with a strong focus on contractual safety arrangements. This role is ideal for professionals experienced in Global and Local Pharmacovigilance Agreements (PVAs) who possess in-depth knowledge of international drug safety regulations and compliance frameworks.
The successful candidate will play a critical role in ensuring that all pharmacovigilance agreements are aligned with regulatory expectations, company standards, and global best practices.
Key Responsibilities
Pharmacovigilance Agreements Management
Draft new Pharmacovigilance Agreements (PVAs) and revise existing agreements in alignment with company policies and regulatory requirements
Review PVAs to ensure quality, accuracy, and consistency with internal standards and global pharmacovigilance regulations
Address and resolve internal and collaborating company comments related to PVA content and compliance
Compliance & Documentation
Maintain and manage the dedicated PVA mailbox to ensure timely communication and documentation tracking
Announce new and revised PVAs to all relevant internal and external stakeholders
Maintain an up-to-date PVA tracker for all active global agreements, including reconciliations and version updates
Upload, archive, and maintain PVAs and supporting documents in the centralized PVA repository
Monitoring & Reporting
Perform compliance monitoring of effective PVAs and prepare dashboards and reports to support oversight activities
Support Project Managers or designated stakeholders in managing and updating project-related trackers and documentation
Participate in team meetings and provide regular status updates, including escalation of any issues identified during PVA operations
Required Experience & Skills
Experience:
Minimum 3–7 years of hands-on experience in Pharmacovigilance
Proven experience working with Global and Local Pharmacovigilance Agreements
Exposure to regulated pharmaceutical and Life Sciences environments
Regulatory Knowledge:
Strong working knowledge of global pharmacovigilance regulations, including ICH guidelines and Good Pharmacovigilance Practices (GVP) modules
Understanding of contractual safety obligations between Marketing Authorization Holders, partners, and vendors
Professional Skills:
Strong attention to detail with excellent documentation and organizational skills
Effective written and verbal communication skills
Ability to collaborate with cross-functional and global stakeholders
Experience working with trackers, dashboards, and compliance monitoring tools
Education
Bachelor of Pharmacy (B.Pharm)
Master of Pharmacy (M.Pharm)
Bachelor of Science (B.Sc)
Master of Science (M.Sc)
Desired Profile
Background in Life Sciences domain with strong exposure to Drug Safety and Pharmacovigilance
Experience supporting global pharmaceutical clients and multi-country safety agreements
Ability to manage multiple PVAs simultaneously in a fast-paced, compliance-driven environment
Why This Role
This position offers an opportunity to work on global pharmacovigilance contracts, contribute to regulatory compliance, and collaborate with international stakeholders. It is well-suited for professionals seeking to strengthen their expertise in PV Agreements, compliance monitoring, and global drug safety operations.
Apply now on thepharmadaily.com
Advance your career in Pharmacovigilance Agreements, Drug Safety Compliance, and Global Life Sciences Operations.
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