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Clinical Research Coordinator - Hematology Oncology (Beverly Hills)

University of California - Los Angeles Health
$38.19-61.45 Hourly
United States, California, Beverly Hills
Nov 07, 2026
Description

The
Clinical Research Coordinator contributes to the overall operational management
of clinicalresearch/trial/study activities from design, set up,
conduct, through closeout. In this role, you will beresponsible for the implementation of research activities
for one or more studies. Perform necessarytasks to manage projects and prioritizes work to meet
necessary deadlines. You will be responsible forplanning and organizing necessary tasks to ensure adherence
to the study protocol and applicableregulations, such as institutional policy and procedures,
FDA Code of Federal Regulations (CFR), andICH Good Clinical Practice (GCP). The Clinical Research
Coordinator collaborates with the PrincipalInvestigator (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 notlimited to, compliant conduct, financial management, and
adequate personnel support.

Hourly salary range: $38.19 - $61.45

Qualifications

Required:

Bachelor's degree in related area and/or equivalent
combination of education and experience.

Minimally 2+ years of previous study coordination or
clinical research coordination experience.

Interpersonal skills to effectively communicate information
in a timely, professional manner and establish and maintain cooperative and
effective working relationships with students, staff, faculty, external
collaborators and administration and to work as a member of a team.

Ability to effectively communicate to and interact with
patients in a compassionate and kind manner.

Ability to set priorities and complete ongoing tasks with
competing deadlines, with frequent interruptions, to meet the programmatic and
department needs, while complying with applicable University policies and
federal and state regulations.

Analytical skills to assess clinical research protocols and
regulatory requirements, define problems, formulate logical solutions, develop
alternative solutions, make recommendations, and initiate corrective actions.

Close attention to detail to ensure accuracy in a
fast-paced, fluctuating workload environment.

Organization skills to create and maintain administrative
and regulatory files effectively as well as independently balance the various
tasks to ensure deadlines are met.

Demonstrated proficiency with Adobe and Microsoft suite
software, especially Excel, to perform daily tasks efficiently and accurately.

A learning and professional growth mentality so that new
software tools, systems, and processes can be adopted quickly and efficiently.

Working knowledge of clinical research concepts, policies
and procedures, and human safety protection regulations and laws.

Knowledge of and experience working with a variety of local
and external IRBs, scientific review and other research committees, national
cooperative group sponsors, industry sponsors, federal and foundation funding
organizations, etc.

Strong verbal and written communication skills to
effectively establish rapport, building collaborative relationships, and
communicate complex concepts and ideas in an easy-to-understand manner.

Ability to adapt to changing job demands and priorities,
remain flexible including working flexible hours to accommodate research
deadlines.

High degree of concentration and focus in a work
environment that contains distracting stimuli, competing deadlines, and work
delegated by more than one individual.

Availability to work in more than one environment,
travelling to various clinic sites, meetings, conferences, etc.

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