• Study Coordinator

    UCLA Health (Los Angeles, CA)


    The Department of Medicine is hiring a Clinical Research Coordinator within the Division of Pulmonary Medicine to support the full lifecycle of clinical research studies, from design and setup to conduct and closeout. This role is responsible for implementing research activities, managing multiple projects, and prioritizing tasks to meet deadlines while ensuring strict adherence to study protocols and regulatory requirements, including institutional policies, FDA regulations, and ICH Good Clinical Practice (GCP).

     

    The Clinical Research Coordinator works closely with research teams, ancillary departments, sponsors, and other stakeholders to ensure smooth study operations. Responsibilities include coordinating study activities, maintaining compliance, supporting financial management, and providing adequate personnel support to ensure the successful execution of clinical trials.

     

    Hourly Range: $35.31-$56.82

    Required:

    + Bachelors Degree or 1-3 years of previous study coordination or clinical research coordination experience

    + 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 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.

    + 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.

    + Working knowledge of the clinical research regulatory framework and institutional requirements.

    DescriptionQualifications

    UCLA Health welcomes all individuals, without regard to race, sex, sexual orientation, gender identity, religion, national origin or disabilities, and we proudly look to each person’s unique achievements and experiences to further set us apart.