Analyst - R&D

Education : EQUIVALENTEXPERIENCE

At 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: Analyst R&D

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.

Your Responsibilities: -

• 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.
  

What You Need to Succeed (minimum qualifications):

• Bachelor’s or master’s degree in related field.
  
• 0-1 year of experience in Basic knowledge of medical terminologies and able to understand common medical terms relevant to pharmacovigilance and adverse event reporting.
  

What will give you a competitive edge (preferred qualifications):

• 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.
  

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