Description
Notes: - HCP required (RN; PharmD)
- 1 year BAU role.
- Recent (2008 to present) safety experience within reviewing clinical trials
REQUIRED. - MD's are over-qualified.
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.
SKILLS
Safety and Risk Management
Synectics is an Equal Opportunity Employer.