Clinical Research Coordinator - Hematology/Oncology (Santa Monica)
UCLA HealthAbout the role
General Information
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Primary Duties and Responsibilities
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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.
Hourly salary range: 38.19 - 61.45
Job Qualifications
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Bachelor's degree in related area and/or equivalent combination of education and experience. (Required)
Minimally 2+ years of previous study coordination or clinical research coordination experience. (Required)
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.Ā (Required)
Ability to effectively communicate to and interact with patients in a compassionate and kind manner. (Required)
Ability t
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