Job details
- Location
- San Francisco, California
- Work type
- Hybrid
- Posted
- 6 days ago
- Apply on
- iazuqy.fa.ocs.oraclecloud.com
About this role
BS/BA in related area or equivalent; project management or coordinator experience; clinical trials regulatory or CRC experience; knowledge of clinical trial design and operations; Microsoft Office proficiency; ability to obtain SoCRA or ACRP certification within one year.
What you'll do at University of California, San Francisco:
- managing clinical trials
- coordinating protocol reviews
- preparing regulatory submissions
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