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United States
UCLA Health Hiring for Clinical Research Coordinator – OBGYN at Los Angeles, CA Full Time
Qualifications
- 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.
