Role: Associate Director, Safety Science at Erasca, supporting safety and pharmacovigilance across oncology molecules in early and late-phase clinical development.
Responsibilities
- oversee signal detection and management activities
- prepare safety documentation (e.g., DSUR, IND reports)
- review clinical protocols and safety data
- contribute to safety assessments
- collaborate with safety operations and external vendors
Requirements
- healthcare professional degree (MD, PharmD, RN)
- 4+ years in drug development with at least 2 years focused on drug safety
- strong understanding of safety science, PV regulations (GVP, GCP), and clinical risk management
Preferred
- experience with safety databases like Oracle Argus
- leadership skills
- effective communication abilities
High Value
- oncology (cancer)
- immuno-oncology
- precision oncology
- molecular targeted therapies
- regulatory safety reporting
- cross-functional clinical trial team interface
Work Setup
- hybrid (San Diego or South San Francisco) or remote U.S.
- no travel specified
Assoc Director Safety Science in san diego at Unknown Company
This position is listed as full time and able to be worked remotely.