Clinical Research Coordinator, CARE Center
University of California - Los Angeles Health | |
United States, California, Los Angeles | |
April 23, 2024 | |
Description
As the Clinical Research Coordinator for the Department of Medicine, CARE Center, you will be responsible for performing research activities directly related to HIV clinical trials and COVID-19 clinical trials. Duties include:
*Coordinate activities for clinical research studies, such as participant recruitment and enrollment; data management; and education as related to each protocol *Document signs, symptoms and other changes with research patients *Assist with preparing reports and submissions *Participate in quality assurance activities for studies across the research unit *Work with outreach team in expanding recruitment efforts for COVID-19 and HIV trials Salary range: $32.65-$52.53 Hourly Qualifications
Required:
* 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 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. * 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. * 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. * Working knowledge of the clinical research regulatory framework and institutional requirements. |