Job descriptionAt Elanco (NYSE: ELAN) – it all starts with animals! As a global leader in animal health, we are dedicated to innovation and delivering products and services to prevent and treat disease in farm animals and pets.
At Elanco, we are driven by our vision of Food and Companionship Enriching Life and our purpose – all to Go Beyond for Animals, Customers, Society and Our People. At Elanco, we pride ourselves on fostering a diverse and inclusive work environment.
We believe that diversity is the driving force behind innovation, creativity, and overall business success.
Here, you’ll be part of a company that values and champions new ways of thinking, work with dynamic individuals, and acquire new skills and experiences that will propel your career to new heights. Making animals’ lives better makes life better – join our team today! Your Role: Associate Manager – PV Case Processing The Associate Manager – PV Case Processing is responsible for performing the assessment, management, and submission of adverse event reports in compliance with global pharmacovigilance regulations and timelines.
This role involves data accuracy, completeness, and quality, manages regulatory submissions, and supports internal and external stakeholders through effective communication and collaboration.
Your Responsibilities: - * Identify issues in case processing that may result in a delay in submission and escalate issues to management as appropriate. * Comply with internal and external timelines for managing adverse events and product complaint case processing, and case submission processes as appropriate. * Validation of data entry against source documents and call notes as appropriate. * Attempt to obtain follow-up information from external parties through effective written and oral communications. * Stay current on global regulatory issues and practices related to GPV. * Understand the confidential nature of company information and take necessary steps to ensure its protection. * * What You Need to Succeed (minimum qualifications): * Veterinarian (equivalent to US DVM degree) with or without pharmacovigilance experience; or bachelor’s degree in pharmacy or Life Sciences related field with 4-7 years of pharmacovigilance experience. What will give you a competitive edge (preferred qualifications): * Strong understanding of medical terms, clinical concepts, and their relevance in adverse event case processing. * Expertise in data entry, validation, and review processes to ensure completeness, accuracy, and quality of adverse event reports. * Ability to establish and maintain effective communication and working relationships with coworkers, managers, and relevant stake holders. * Willingness and aptitude to learn new skills in the field of safety. * Team player with the ability to contribute and work towards achieving team goals. * Ability to support during high volumes and flexibility to work extended hours when required. Additional Information: * Travel: 0% * Location: India, Bangalore Don’t meet every single requirement? Studies have shown underrecognized groups are less likely to apply to jobs unless they meet every single qualification.
At Elanco we are dedicated to building a diverse and inclusive work environment.
If you think you might be a good fit for a role but don't necessarily meet every requirement, we encourage you to apply.
You may be the right candidate for this role or other roles! Elanco is an EEO/Affirmative Action Employer and does not discriminate on the basis of age, race, color, religion, gender, sexual orientation, gender identity, gender expression, national origin, protected veteran status, disability or any other legally protected status Elanco may use automated tools, including AI, to support parts of our recruitment process, such as reviewing applications against job‑related criteria and/or transferrable skills.
These tools help ensure a consistent, structured evaluation, but they do not make hiring decisions.
All decisions involve a human reviewer.
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