Senior Drug Safety Associate
Where
- South San Francisco, CA
What you'll be doing
- Receives and reviews adverse event forms for completeness, recognizes discrepancies, enters data into safety database, obtains follow up information and assesses causal relationship of event to drug. Abilities to set work priorities and directions with input from manager. Acts as a trainer and mentor for more junior global drug safety staff. Full case processing experience, including initial intake, triaging, narrative writing and submissions. Performs MedDRA, WHO-DD and other medical dictionary coding of clinical trial data from the clinical database in collaboration with data management and clinical science.
What your background should be
- Has at least 3+ years of clinical case processing experience (post market experience is a plus as well). Familiarity and experience with oncology or other high risk therapeutic areas is preferred. Has participated in study execution team (SET) and similar meetings, representing the drug safety department.
Required Schooling / Training
- Bachelor degree in the sciences. Medical degree (BSN, MD, PharmD) is preferred but not required.
Who is the client company
- This is an international staffing and workforce management company.
- If you are interested in this position, send your resume to apply@kochdavis.com
