Associate Manager - PV Case Processing
Core
Assess, manage, and submit adverse event reports in compliance with global pharmacovigilance regulations.
Role type
Associate Manager, Pharmacovigilance Case Processing
Builds
Adverse event reports and regulatory submissions
Domain
Animal health / Pharmacovigilance
Required skills
Adverse event case processing, Regulatory compliance, Data validation, Stakeholder communication, Issue escalation, Global regulatory knowledge
Preferred skills
Medical terminology, Clinical concepts, Data entry expertise, High-volume support, Flexibility for extended hours
Technologies
None stated
Responsibilities
Identify processing delays and escalate to management; Comply with internal and external timelines for adverse event and complaint case processing; Validate data entry against source documents and call notes; Obtain follow-up information from external parties via written and oral communication; Stay current on global regulatory issues and practices related to GPV; Ensure protection of confidential company information.
