New

Clinical Research Coordinator

University of California - Los Angeles Health
United States, California, Los Angeles
Jul 23, 2026
Description The Department of Medicine is seeking a Clinical Research Coordinator to support the planning, coordination, and implementation of clinical research studies across the full study lifecycle, from start-up and participant enrollment through study closeout. The Clinical Research Coordinator will work closely with Principal Investigators (PIs), research staff, sponsors, and institutional partners to ensure the efficient and compliant conduct of research activities. Responsibilities include coordinating study operations, maintaining regulatory and study documentation, monitoring study progress and timelines, facilitating communication among key stakeholders, and ensuring adherence to study protocols, institutional policies, FDA regulations, and Good Clinical Practice (GCP) guidelines. The successful candidate will demonstrate strong organizational and project management skills, the ability to prioritize competing responsibilities, and a commitment to advancing high-quality clinical research in a collaborative academic environment. Hourly range: $38.19-$61.45 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.