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Research Assistant - Family Medicine

University of California - Los Angeles Health
United States, California, Los Angeles
Apr 10, 2026
Description

The UCLA Department of Family Medicine is seeking a motivated Research Assistant to join a dynamic and fast-paced team of highly experienced primary care physicians and researchers with a passion to improve patient health. Under the direction of the Principal Investigator and Project Manager, this position will primarily support patient recruitment for a PCORI-funded, nationwide multi-year, multi-site clinical trial around acute sinusitis but will also touch on other NIH-funded research projects related to preventive health care for older adults.

Responsibilities include developing relationships with and coordinating with clinic staff and providers across multiple primary/urgent care offices to identify eligible patients, recruiting patients to enroll, conducting in-person patient screening, obtaining informed consent, completing participant enrollment procedures, performing participant follow-ups, performing data quality checks, organizing medication deliveries to participants, and sending and tracking participant incentives. Candidates may also need to meet with patients outside of the clinic to perform enrollment procedures. Candidates will also be responsible for regular communication with the study team, reporting in team meetings about recruitment progress, identification of strategies to improve recruitment, and participation in larger team calls with all participating sites. Candidates may also be asked to prepare monthly reminder call schedules, meeting agendas, develop written protocols and maintain FAQ documents. Other tasks may include generating figures for reports, coding and analyzing semi-structured interviews using qualitative analysis software, managing data, and reviewing the scientific literature. This position also will perform miscellaneous administrative duties related to research, such as scheduling, taking meeting notes, and coordination and verification of transcriptions.

Please note that this is a full time one year limited position and may
convert to career
.

Salary Range: $36.37 - $58.52/Hourly

Qualifications

All Required:

  • Bachelors Degree or
    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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