Description
The Drug Safety Associate 2 encompasses a key role in the day-to-day functioning of the Pharmacovigilance and Drug Safety department.Responsible for all aspects of adverse event processing and reporting for assigned investigational and marketed products, while maintaining compliance with SOPs and FDA, ICH and worldwide regulations to ensure uniform and timely processing and reporting of adverse event reports.
Serves as a liaison to external healthcare providers, investigational sites, and company personnel for safety-related issues, working in close collaboration with colleagues from Clinical Science, Clinical Operations, Biometrics, Regulatory & QA, MedSA and Commercial.
Work Experience:
- 2-3 years of Pharmacovigilance / Drug Safety experience or equivalent required, specifically in a global environment
Oncology experience preferred
To find out more about Real please visit www.realstaffing.com