Assistant Regulatory Affairs Coordinator

University of California System•Orange, CA

33d•$27 - $44•Hybrid

About The Position

The Assistant Regulatory Affairs Coordinator position will work directly with the Lead Regulatory Coordinator to ensure successful management of the regulatory aspects of each study conducted through UCI's Center for Clinical Research. This position will work a hybrid, onsite/from home, schedule and report on site to both Irvine and Orange offices as directed.

Requirements

Ability to prioritize assignments and achieve high productivity/quality with short time frames, under rigid deadlines, and/or in environments with frequent workload changes and competing demands
Maintains high level of professionalism as this role requires staff to be the "face" of the study to various stakeholders including industry study sponsors, CROs, PIs, and other study collaborators. Failure to do so would result in affecting relationships and reputation of the unit and affect future collaborations.
Excellent problem-solving skills and quick-thinker capabilities
Proficient in Microsoft Office to be able to generate reports and documents in Word, Excel and PPT
Basic understanding of clinical trials/research
Strong communication skills as this role requires constant contact with all study stake holders including study sponsors, CROs, PIs, and various units within the department
Possess a high degree of accuracy, detail-orientated, self-motivated and available for flexible scheduling
HS graduation and sufficient experience and demonstrated skills to successfully perform the assigned duties and responsibilities.
Must be able to commute to the Orange and Irvine location. This position is onsite.