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 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.
Preferred
Bachelors Degree or 1-3 years of previous study coordination or clinical research coordination experience.
Seniority level
Entry level
Employment type
Full-time
Job function
Research, Analyst, and Information Technology
Industries
Hospitals and Health Care
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