Description
UCLA HEALTH
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Description
The
Clinical Research Coordinator supports the operational management of clinical
research activities throughout the study lifecycle, including design, start-up,
conduct, and closeout. This role is responsible for implementing and managing
research activities for one or more studies, prioritizing tasks to meet
required deadlines. The Coordinator plans and organizes study activities to ensure
compliance with study protocols and applicable regulations, including
institutional policies, FDA Code of Federal Regulations (CFR), and ICH Good
Clinical Practice (GCP). The role involves close collaboration with the
Principal Investigator, ancillary departments, central research teams, sponsors,
and external institutions to support compliant study conduct, financial
management, and adequate staffing.
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. - Working knowledge of the clinical research
regulatory framework and institutional requirements. - 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. - 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.