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.
QUALIFICATIONS:
HCP IS REQUIRED. Previous drug safety experience is preferred; Foreign MD's will be considered; Industry experience and past drug safety experience is highly desired.
SKILLS
MS Excel, MS Outlook, Safety and Risk Management
Synectics is an Equal Opportunity Employer.