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. 

Veterinarian (equivalent to US DVM degree) with or without pharmacovigilance experience; or bachelor’s degree in pharm...