Associate Manager – Pharmacovigilance Case Processing
Location: Bengaluru, Karnataka, India
Employment Type: Full-Time
Experience Required: 4–7 years
Job Requisition ID: R0023344
Industry: Animal Health | Pharmacovigilance | Drug Safety
Job Overview
Elanco, a global leader in animal health, is hiring an Associate Manager – Pharmacovigilance Case Processing to support end-to-end adverse event case management and regulatory submissions. This role is critical in ensuring the timely, accurate, and compliant processing of safety cases in accordance with global pharmacovigilance regulations.
The position is ideal for experienced pharmacovigilance professionals with strong expertise in case intake, data quality, follow-up, and regulatory timelines, particularly within a fast-paced, compliance-driven environment.
Key Responsibilities
PV Case Processing & Regulatory Compliance
Perform assessment, processing, and submission of adverse event reports in pharmacovigilance safety databases in line with global regulatory requirements.
Ensure data accuracy, completeness, and quality throughout the case lifecycle.
Manage regulatory reporting timelines and ensure on-time submissions to relevant Health Authorities.
Case Management & Quality Control
Validate safety data entered into the PV database against source documents, call notes, and supporting materials.
Identify potential issues that may impact submission timelines and escalate risks proactively to management.
Support the management of product complaint and adverse event cases, as applicable.
Follow-Up & Stakeholder Communication
Obtain follow-up information from reporters, healthcare professionals, or external stakeholders through effective written and verbal communication.
Collaborate with internal teams and cross-functional stakeholders to resolve data gaps and case quality concerns.
Required Skills & Competencies
Strong understanding of medical terminology, clinical concepts, and adverse event case processing
Hands-on experience with PV safety databases and regulatory reporting workflows
High attention to detail with a strong focus on data quality and compliance
Ability to work independently while adhering to established SOPs and global guidelines
Effective communication and stakeholder management skills
Adaptability to evolving processes and regulatory expectations
Qualifications & Experience
Educational Background: Life Sciences, Pharmacy, Veterinary Sciences, or a related discipline (preferred)
Experience:
4 to 7 years of experience in Pharmacovigilance Case Processing, including adverse event management and regulatory submissions
Additional Information
Work Location: Bengaluru, India
Travel Requirement: None
Work Model: Onsite / Hybrid (as per business requirements)
Why Join Elanco
Work with a globally recognized animal health organization
Contribute to products that improve animal health and well-being worldwide
Be part of an inclusive, innovation-driven culture
Gain exposure to global pharmacovigilance operations and regulatory frameworks
Equal Opportunity Statement
Elanco is an Equal Opportunity and Affirmative Action Employer. Employment decisions are made without regard to age, race, color, religion, gender, sexual orientation, gender identity or expression, national origin, disability, veteran status, or any other legally protected status.
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