Description
UCLA HEALTH
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Description
The
Department of Surgery is seeking an experienced Clinical Research Coordinator
to support interventional clinical trials across multiple divisions. This role
will be responsible for coordinating and managing study activities for both
drug and device trials, including participant recruitment, study implementation,
data collection, and ensuring compliance with all regulatory requirements, institutional
policies, and study protocols.
Hourly Salary Range: $36.37 – $58.52
Qualifications
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. Al Required - 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.