Provide statistical programming and validation for clinical trial datasets, work with external vendors, and ensure statistical programming quality and accuracy.

The Pharmacovigilance Specialist manages adverse event case processing, ensures regulatory compliance, performs follow-ups, and contributes to training and quality reviews.

The Senior Pharmacovigilance Coordinator manages daily processing of adverse event cases, ensuring accuracy and compliance. Responsibilities include case follow-ups, reviews, and developing training materials while maintaining an up-to-date knowledge of global safety regulations.