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Research Assistant - Hematology/Oncology (Santa Monica)

University of California - Los Angeles Health
United States, California, Santa Monica
Jun 25, 2026
Description

The Assistant Clinical Research Coordinator assists the Clinical Research Coordinator and/orSenior Clinical Research Coordinator in contributing to the overall operational management ofclinical research/trial/study activities. In this role, you will perform necessary tasks to assist inmanaging projects and prioritizing work to meet necessary deadlines. You will provide support in planning and organizing necessary tasks to ensure adherence to the study protocol and applicable regulations.

Hourly salary range: $30.74 - $49.46

Qualifications

Required:


  • Minimum of 1+ years of
    experience in a clinical research setting
  • 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.
  • Ability to handle confidential
    information with judgement and discretion.
  • 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.

Preferred:


  • Bachelor's Degree in related
    area and/or equivalent combination of education and experience
Applied = 0

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