CLINICAL TRIALS COORDINATOR - UROLOGY
Company: University of California
Location: Los Angeles
Posted on: October 23, 2024
Job Description:
Description The Department of Urology is seeking to hire a full
time Clinical Research Coordinator. Under the direct supervision of
the Clinical Trials Administrator, the Clinical Research
Coordinator contributes to the overall operational management of
clinical research / trial / study activities from design, set up,
conduct, through closeout. The ideal candidate is an experienced
professional 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. In this role you will:
- Recognize and perform necessary tasks to manage projects and
prioritizes work to meet necessary deadlines.
- 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).
- Collaborate 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. Please note that the salary will be determined
based on various factors including, but not limited to,
qualifications, experience, and equity. Pay Range: $ Qualifications
- 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.
Keywords: University of California, Monterey Park , CLINICAL TRIALS COORDINATOR - UROLOGY, Healthcare , Los Angeles, California
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