UCLA Health Los Angeles, CA, USA
Responsibilities Under the direction of the Operational Managers, Investigators, Financial Administrative Office, Faculty, Medical and Administrative Directors of the Jonsson Comprehensive Cancer Center (JCCC) Clinical Research Unit (CRU) the Regulatory Research Associate will participate in UCLA Main Campus research activities as part of the regulatory team. In this role, you will be responsible for preparation, submission, and maintenance of regulatory applications to fulfill research requirements for open studies in addition to working with Sponsor monitors to timely process, review, and collect regulatory documents maintained in the Investigator Site File. All work should be completed according to Good Clinical Practice, JCCC CRU standard operating policies, UCLA Institutional Review Board (IRB) and government regulations. Qualifications Required: • Demonstrated knowledge of “good clinical practices” for clinical research as defined by the Code of Federal...