California Licensed Drug Safety Associate

Job Summary

A company is looking for a Drug Safety Associate III.

Key Responsibilities

• Process and assess serious adverse events (SAEs) in the Argus database, including case closure and narrative writing
• Collaborate with various departments to ensure proper collection and handling of safety data
• Perform Safety Study Lead activities, including the development of safety management plans and SAE reconciliation

Required Qualifications, Training, and Education

• BS/BA in Nursing, Pharmacy, or related discipline with a minimum of 7 years of experience; or MS/MA with 5 years; or PhD with no experience
• Experience in the Biotech/Pharmaceutical industry, preferably in oncology
• Experience using the Argus safety database is preferred
• Clinical trial and spontaneous adverse event processing experience is required
• May require certification in the assigned area