Clinical Trials Regulatory Associate

Cedars-Sinai Outpatient Cancer Center at the Samuel Oschin Comprehensive Cancer Institute is seeking a:

 

Clinical Trials Regulatory Associate

(Full-Time)

 

This position is primarily responsible for supporting the Research Department’s regulatory filings, Institutional Review Board (IRB) submissions, and reporting and file maintenance efforts. Key functions will also include completing all forms and generating all reports necessary to comply with regulatory and IRB requirements and company policies. Requires 3+ years experience in providing administrative support in a clinical research or other similar and technical environment. Must have knowledge of typical office software applications and database programs, sufficient to generate routine correspondence, and moderately complex spreadsheet and multimedia presentations and reports.

 

We offer a competitive salary & benefits plan. For immediate consideration, please mail/fax/email resume to: HR Manager, 50 North La Cienega, Suite 350, Beverly Hills, CA 90211. FAX (310) 360-7128. E-mail: ella.carlisle@cshs.org . EOE.