What are the responsibilities and job description for the Study Coordinator - Neurology position at UCLA Health System?
Description The Clinical Research
Coordinator plays a critical role in the overall operational management of
clinical research/trial/study activities from design, set up, conduct, through
closeout. The incumbent is an experienced professional or leader who has direct
responsibility for the implementation of research activities for one or more
studies which may include multicenter clinical trials (both NIH and
industry-sponsored), local investigator-initiated clinical trials, and/or
programmatic clinical research activities. The incumbent recognizes and
performs necessary project management tasks and prioritizes work to reach
scheduled goals. The incumbent is a technical leader responsible for ensuring
the study protocol and procedures have been completed accurately, safely, and
in a timely manner. This position may supervise and train others on projects as
necessary. The incumbent works with PIs, departments, sponsors, institutions,
and other entities as needed to support and provide guidance on the
administration of the compliance, financial, personnel and other related
aspects of studies.
Hourly salary range: 38.19
- 61.45.
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.
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.
$38.19-61.45 Hourly Monday-Friday 8am-5pm
Salary : $38 - $61