Associate Manager - PV Case Processing

Roles & Responsibilities
• Assess, manage, and submit adverse event (AE) reports in the pharmacovigilance (PV) database
• Ensure compliance with global PV regulations and reporting timelines
• Identify potential case processing delays and escalate issues to management
• Manage product complaint case processing and regulatory submissions as required
• Validate data entry against source documents and call notes for accuracy and completeness
• Follow up with external parties to obtain missing or additional safety information
• Maintain high-quality standards in adverse event documentation and submission
• Support internal and external stakeholders through effective communication and collaboration
• Ensure adherence to SOPs, policies, and regulatory requirements

Qualification
• Relevant educational background or equivalent experience in Life Sciences, Pharmacy, Veterinary Sciences, or related field

Experience
• 4–7 years of experience in Pharmacovigilance case processing
• Experience in adverse event data entry, validation, and regulatory submissions

Skills
• Strong understanding of medical terminology and clinical concepts
• Expertise in data entry, validation, and quality review processes
• Ability to follow guidelines and work independently
• Strong communication and stakeholder management skills
• Flexibility and adaptability in a dynamic process environment
• Willingness to learn and grow within the safety domain

About the Company
Elanco is a global leader in animal health dedicated to preventing and treating disease in farm animals and pets. Guided by its vision of Food and Companionship Enriching Life, Elanco focuses on innovation, diversity, and improving the well-being of animals, customers, and communities worldwide.