Elanco Animal Health Hiring PV Case Processing Analyst

Elanco Animal Health Incorporated is an American pharmaceutical company which produces medicines and vaccinations for pets and livestock. Until 2019, the company was a subsidiary of Eli Lilly and Company, before being divested. It is the third-largest animal health company in the world.

Post : Analyst - GDPS

The Analyst in PV Case Processing is responsible for managing adverse event reports, ensuring data accuracy, and maintaining compliance with global pharmacovigilance regulations and timelines. The role involves data entry, assessing seriousness and causality, and ensuring the completeness and quality of cases for regulatory submission. Effective communication skills, knowledge of regulations, and the ability to manage multiple priorities are essential. The Analyst must demonstrate Elanco core values, adaptability, and commitment to high-quality standards in all tasks.

Your Responsibilities
Adverse Event Case Processing
• Responsible for data entry, seriousness assessment and causality assessment of adverse event reports in the PV database
• Identifies issues in case processing that may result in a delay in submission and escalates issues to management as appropriate.
• Develop an understanding of pharmacovigilance regulations.
• Comply with internal and external timelines for managing adverse events and product complaint case processing, and case submission processes as appropriate.
Typical case processing activities include (but not limited to) :
• Validation of data entry against source document(s) and call notes as appropriate.
• Assessment of adverse event reports for seriousness, reportability's and causality including reason for assessment.
• Perform self-review of all data for completeness, correctness and quality.
• Ensuring that the case is considered complete, accurate, and ready for submission to appropriate regulatory authorities.
• Determine what, if any, follow-up information is needed
• Ensure to meet the expected productivity and quality standards.
• Active participation in team meetings.
• Perform other duties as assigned.

Key Technical Responsibilities :
• Basic knowledge of medical terminologies and able to understand common medical terms relevant to pharmacovigilance and adverse event reporting.
• Effective verbal and written communication skills to liaise with internal and external stakeholders.
• Ability to work effectively on multiple products and effectively manage priorities.
• Ability to establish and maintain effective working relationships with coworkers, managers and relevant stake holders.
• Capable of adhering to applicable, global, local regulatory requirements.
• Skill in using multiple databases. Ability to support during high volumes and flexibility to work extended hours when required. Self-motivated, flexible, and receptive to changes.

Candidate Profile
Veterinarian (equivalent to US DVM degree) with or without pharmacovigilance experience and M.Pharm with Pharmacovigilance Experience : 0-2 years of pharmacovigilance experience.

Additional Information
Experience : 0-2 years
Qualification : M.Pharm
Location : Bangalore
Industry Type : Pharma/ Healthcare/ Clinical research
Job ID : R0026397
End Date : 30th September 2026