Strong verbal and written communication skills along with strong interpersonal skills to effectively establish rapport, and build collaborative relationships.
Strong organizational capabilities to organize multiple projects and competing deadlines for efficiency and cost-effectiveness.
Ability to adapt to changing job demands and priorities; work flexible hours to accommodate research deadlines.
Typing and computer skill/ability including word-processing, use of spreadsheets, email, data entry.
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.
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.
Typing and computer skill/ability including word-processing, use of spreadsheets, email, data entry. Ability to navigate numerous software programs and applications.
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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