Description The Clinical Research Coordinator contributes to the overall
operational management of clinical research/trial/study activities from design,
set up, conduct, through closeout. In this role, you will be responsible for
the implementation of research activities for one or more studies. Perform
necessary tasks to manage projects and prioritizes work to meet necessary
deadlines. You will be responsible for planning and organizing necessary tasks
to ensure adherence to the study protocol and applicable regulations, such as
institutional policy and procedures, FDA Code of Federal Regulations (CFR), and
ICH Good Clinical Practice (GCP). The Clinical Research Coordinator
collaborates with the Principal Investigator (PI), ancillary departments,
central research infrastructure teams, sponsors, institutions, and other
entities as needed to support the administration of all aspects of studies,
including, but not limited to, compliant conduct, financial management, and
adequate personnel support.
Salary offers are determined based on various factors including,
but not limited to, qualifications, experience, and equity. UCLA Health hourly
salary range for this position is $33.63- $54.11.
Qualifications Required :
Bachelor's
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 be flexible in handling work delegated by more than one individual.
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.
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