Description The Department of Urology is seeking to hire a full time Clinical Research Coordinator to contribute to the overall operational management of clinical research / trial / study activities from design, set up, conduct, through closeout. The position has responsibility for the implementation of research activities for one or more studies. You'll recognize and perform necessary tasks to manage projects and prioritizes work to meet necessary deadlines. Duties will include: + Planning and organizing necessary tasks to ensure adherence to the study protocol and applicable regulations, such as institutional policy and procedures, FDA Code of Federal Regulations (CFR), and ICH Good Clinical Practice (GCP). + Coordinator collaborates with the Principal Investigator (PI), ancillary departments, central research infrastructure teams, sponsors, institutions, and other entities as needed to support the administration of all aspects of studies, including, but not limited to, compliant conduct, financial management, and adequate personnel support. + Other duties as assigned. Pay Range: $33.63 - $54.11 hourlyQualifications Bachelors Degree or 1-3 years of previous study coordination or clinical research coordination experience All Essential Strong verbal and written communication skills along with strong interpersonal skills to effectively establish rapport, and build collaborate relationships. All Essential Strong organizational capabilities to organize multiple projects and competing deadlines for efficiency and cost-effectiveness. All Essential Analytical skills sufficient to work and solve address problems and identify solutions with reasoned judgment. All Required Ability to adapt to changing job demands and priorities; work flexible hours to accommodate research deadlines. All Required Ability to respond to situations in an appropriate and professional manner. All Required Ability to concentrate and focus in a work environment that contains distracting stimuli and competing deadlines. All Required Ability to be flexible in handling work delegated by more than one individual. All Required Typing and computer skill/ability including word-processing, use of spreadsheets, email, data entry. Ability to navigate numerous software programs and applications. All Required Ability to handle confidential material information with judgement and discretion. All Required Working knowledge of the clinical research regulatory framework and institutional requirements. All Essential 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. All Required Working knowledge of FDA Code of Federal Regulations (CFR) and ICH Good Clinical Practice (GC) for clinical research. All Required Be available to work in more than one environment, travel to meetings, off-site visits, conferences, etc. All Required UCLA Health welcomes all individuals, without regard to race, sex, sexual orientation, gender identity, religion, national origin or disabilities, and we proudly look to each person’s unique achievements and experiences to further set us apart.