Required:
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.
University of California - Los Angeles Health
Aug 04, 2026