The Senior Safety Associate (SSA) is responsible for managing safety reports originating from the company's clinical trials, post-marketing observational studies as well as spontaneous reports in the post-marketing setting. The SSA will be responsible for the timely evaluation and processing of adverse event reports while complying with global safety guidelines and regulations. The SSA will also ensure accurate reporting of adverse event data to regulatory agencies and clinical trial investigator sites worldwide as applicable. |
Preferably nursing or pharmacy or other health related science.
Minimum Bachelors level
Biogen Idec - 19 months ago
Biogen Idec (NASDAQ: BIIB) is a global leader in the discovery, development and delivery of innovative therapies to improve the lives of...