Analyst - R&D
3 days ago
Role Overview: At Elanco, as an Analyst in R&D, you will be responsible for managing adverse event reports, ensuring data accuracy, and maintaining compliance with global pharmacovigilance regulations and timelines. Your role will involve data entry, seriousness assessment, causality assessment, 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 for this position. Key Responsibilities: - Responsible for data entry, seriousness assessment, and causality assessment of adverse event reports in the PV database. - Identify issues in case processing that may result in a delay in submission and escalate issues to management as appropriate. - Develop an understanding of pharmacovigilance regulations. - Ensure compliance with internal and external timelines for managing adverse events and product complaint case processing and case submission processes as appropriate. Qualification Required: - Bachelor's or master's degree in a related field year of experience with basic knowledge of medical terminologies and the ability to understand common medical terms relevant to pharmacovigilance and adverse event reporting. Additional Information: At Elanco, we are committed to fostering a diverse and inclusive work environment where diversity drives innovation, creativity, and overall business success. Join us in making animals" lives better to make life better. Travel required: 0%. Location: India, Bangalore. Note: If you do not meet every single requirement listed, we encourage you to apply as we are dedicated to building a diverse and inclusive work environment. You may be the right candidate for this role or other roles at Elanco.,
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