The Laboratory Center Specialist for regulatory coordination of clinical research studies within assigned units, departments or divisions. They will perform detailed review of clinical research protocols and utilize that information to prepare, manage and submit all required study/regulatory documents and all required applications and forms related to internal UCLA requirements, FDA requirements, sponsor requirements, etc. They will work with study monitors to process, review and collect the appropriate regulatory documents in a timely manner and in compliance with federal, state, and university mandated laws, regulations, and policies.  The Laboratory Center Specialist will rely on past experience in processing PBMCs for NIH sponsored trials when interfacing with clinical trials site processing labs and network proficiency testing subject matter experts.

This is a full-time, 12 month contract position that may convert to career.

Salary Range: $76,200 – 158,800 Annually