Associate Manager – Pharmacovigilance Case Processing
Location: Bangalore, Karnataka, India
Employment Type: Full-Time
Function: Pharmacovigilance | Drug Safety | Animal Health
Industry: Pharmaceutical / Animal Health
Job Overview
Elanco, a global leader in animal health and veterinary pharmaceuticals, is hiring an Associate Manager – PV Case Processing to support its global pharmacovigilance operations in Bangalore. This role is responsible for the accurate assessment, processing, and timely submission of adverse event reports in compliance with global safety regulations.
The position is well-suited for experienced pharmacovigilance professionals or veterinarians seeking leadership exposure within a regulated global safety environment.
Key Responsibilities
Perform end-to-end pharmacovigilance case processing, including assessment, documentation, and submission of adverse event reports
Ensure compliance with global PV regulations, internal SOPs, and submission timelines
Identify potential case processing issues that may impact reporting timelines and proactively escalate to management
Validate case data against source documents, call notes, and supporting records to ensure data accuracy and completeness
Conduct follow-ups with external reporters and stakeholders using effective written and verbal communication
Stay current with global pharmacovigilance regulations, guidance, and best practices
Maintain strict confidentiality of safety data and company information
Collaborate with internal teams and external partners to support high-quality safety reporting
Support case processing activities during high-volume periods, including flexibility for extended hours when required
Required Qualifications & Experience
Veterinarian (equivalent to a US DVM degree) with or without prior pharmacovigilance experience
OR
Bachelor’s degree in Pharmacy, Life Sciences, or a related discipline with 4–7 years of hands-on pharmacovigilance case processing experience
Preferred Skills & Competencies
Strong understanding of medical terminology, clinical concepts, and adverse event evaluation
Expertise in case data entry, validation, quality review, and regulatory compliance
Proven ability to communicate effectively with cross-functional teams, managers, and external stakeholders
High attention to detail with a strong commitment to data quality and regulatory accuracy
Willingness to learn and adapt within a dynamic drug safety environment
Team-oriented mindset with the ability to contribute toward shared safety and compliance goals
Ability to manage workload effectively during peak volumes
Why Join Elanco
Work with a global leader in animal health and veterinary innovation
Exposure to international pharmacovigilance regulations and global safety operations
Inclusive, diverse, and growth-focused work culture
Opportunity to develop leadership skills within drug safety and regulatory compliance
Additional Details
Work Location: Bangalore, India
Travel Requirement: None
Equal Opportunity Employer: Elanco is committed to diversity, equity, and inclusion across all hiring practices
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