Description
Description:Provides support for the review of potential adverse events of products. Reviews and assesses domestic/international clinical trials and post-marketing surveillance AE reports on marketed products. Determines regulatory reporting requirements based on assessments of seriousness and labeling of selected adverse events (AE) terms. Industry experience and past drug safety experience is highly desired.
Notes:
- HCP required (RN, PharmD)
- Recent safety experience within reviewing clinical trials is HIGHLY DESIRED.
Drug safety experience in a pharma setting is REQUIRED. ARGUS experience is REQUIRED.
SKILLS
Clinical Trial Safety Reporting
Synectics is an Equal Opportunity Employer.