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    Research Coordinator - San Antonio, United States - UT Health San Antonio

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    Description

    Job Summary:


    Under general supervision, provides routine technical assistance in performing assigned and delegated tasks in support of clinical research projects with a focus on patient enrollment, data, and biospecimen collection.


    Education:

    • Bachelor's in a basic or applied clinical science is required with a degree in public health preferred.

    Experience:

    • Three (3) years of progressive experience in grant administration, research coordination, data collection, and/or facilitating the patient experience in research projects is required. Previous clinical research project experience is preferred.

    Job Duties:

    • Screens participants for eligibility, obtains informed consent, completes patient enrollment, and follow up.
    • Collects and processes different types of biospecimens (for example: urine, stool, blood, nasal swabs, etc.).
    • Assists with research projects of limited complexity for clinical and population science.
    • Interviews participants and abstracts data from medical charts into standardized case report forms.
    • Provides routine technical assistance in performing assigned and delegated tasks in support of research projects.
    • Performs assigned clerical and technical duties in a research or clinical lab setting.
    • Performs routine tasks with direction from supervisor, manager, or higher-level technician.
    • Carries out general laboratory inventory and maintenance.
    • Coordinates multiple research protocols and grant submissions.
    • Assists with monitoring budgets, spending, purchasing and participant payments.
    • Creates, completes, and tracks forms and reports for study sponsors.
    • Maintains research subject files for each clinical study and enters all subject data into research database.
    • Monitors ongoing activities on various research studies to ensure compliance with local, state & federal regulations.
    • Performs all other duties as assigned.

    Additional Licenses and Certification:

    • Certified Clinical Research Professional (CCRP) is preferred.


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