Analyst - GDPS

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-GDPS

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.

The Analyst must demonstrate Elanco core values, adaptability, and commitment to high-quality standards in all tasks.

Your Responsibilities: -

Adverse Event Case Processing -

·         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.

Typical case processing activities include (but not limited to):


* Validation of data entry against source document(s) and call notes as appropriate.


* Assessment of adverse event reports for seriousness, reportability's and causality including reason for assessment.


* Perform self-review of all data for completeness, correctness and quality.


* Ensuring that the case is considered complete, accurate, and ready for submission to appropriate regulatory authorities.


* Determine what, if any, follow-up information is needed


* Ensure to meet the expected productivity and quality standards.


* Active participation in team meetings.


* Perform other duties as assigned.

Key Technical Responsibilities:

·         Basic knowledge of medical terminologies and able to understand common medical terms relevant to pharmacovigilance and adverse event reporting.

·         Effective verbal...