New

Clinical Research Coordinator - Surgery

University of California - Los Angeles Health
United States, California, Los Angeles
Mar 27, 2026
Description The Department of Surgery, Liver and Pancreatic Transplant Division is seeking an experiencedClinical Research Coordinator to support clinical research studies. This position will assist thePrincipal Investigator in the successful execution and oversight of research activities, including the coordination and management of multiple clinical trials, while ensuring compliance with allapplicable regulatory requirements, and institutional policies. Hourly salary range: $36.37 - $58.52 Qualifications Required: Bachelors Degree or 1-3 years of previous study coordination or clinical research coordination experience Strong verbal and written communication skills along with strong interpersonal skills to effectively establish rapport, and build collaborate relationships. Strong organizational capabilities to organize multiple projects and competing deadlines for efficiency and cost-effectiveness. Analytical skills sufficient to work and solve address problems and identify solutions with reasoned judgment. Ability to adapt to changing job demands and priorities; work flexible hours to accommodate research deadlines. Ability to respond to situations in an appropriate and professional manner. Ability to concentrate and focus in a work environment that contains distracting stimuli and competing deadlines. Ability to be flexible in handling work delegated by more than one individual. Typing and computer skill/ability including word-processing, use of spreadsheets, email, data entry. Ability to navigate numerous software programs and applications. Ability to handle confidential material information with judgement and discretion. Working knowledge of the clinical research regulatory framework and institutional requirements. Mathematical skills sufficient to prepare clinical research budgets, knowledge of math ability and knowledge of clinical trials research budgeting process to assist with the preparation of clinical trial budgets. Working knowledge of FDA Code of Federal Regulations (CFR) and ICH Good Clinical Practice (GC) for clinical research. Be available to work in more than one environment, travel to meetings, off-site visits, conferences, etc.