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    Clinical Research Coordinator I - Boston, United States - Massachusetts General Hospital

    Massachusetts General Hospital
    Massachusetts General Hospital Boston, United States

    2 weeks ago

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    Description

    GENERAL SUMMARY/ OVERVIEW STATEMENT:
    The Dashti Lab ) in the Department of Anesthesia, Critical Care and Pain Medicine at MGH leads clinical and translational nutrition research focused on the sleep and circadian rhythms of patients with nutrition-related challenges.

    The goal of this research is to provide tailored medical treatments and therapies that are less disruptive to sleep and circadian rhythms across diverse patient populations.

    As a member of the Dashti lab, the Clinical Research Coordinator I provides support for ongoing nutrition research projects.

    In working closely in collaboration with other members of the lab, the CRC will be responsible for managing recruitment of patients in multiple nutrition-focused clinical trials (inpatient/outpatient), participating in data collection and entry, as well as ensuring compliance with federal, state and institutional guidelines.

    A description of ongoing projects can be found on the lab website. Prior clinical research experience including experience with clinical nutrition research is strongly preferred. Excellent communication and attention to detail is a must. Two year commitment is strongly preferred.


    PRINCIPAL DUTIES AND RESPONSIBILITIES:
    Please note, the functions below are representative of major duties that are typically associated with these positions. Specific responsibilities may vary based upon departmental needs. Similarly, not all duties that have been outlined will be assigned to each position.


    • Collects & organizes patient data
    • Maintains records and databases
    • Uses software programs to generate graphs and reports
    • Assists with recruiting patients for clinical trials
    • Obtains patient study data from medical records, physicians, etc.
    • Conducts library searches
    • Verifies accuracy of study forms
    • Updates study forms per protocol
    • Documents patient visits and procedures
    • Assists with regulatory binders and QA/QC procedures
    • Assists with interviewing study subjects
    • Administers and scores questionnaires
    • Provides basic explanation of study and in some cases obtains informed consent from subjects
    • Performs study procedures, which may include phlebotomy.
    • Assists with study regulatory submissions
    • Writes consent forms
    • Verifies subject inclusion/exclusion criteria
    • Performs administrative support duties as required

    SKILLS/ABILITIES/COMPETENCIES REQUIRED:

    • Careful attention to details
    • Good organizational skills
    • Ability to follow directions
    • Good communication skills
    • Computer literacy
    • Working knowledge of clinical research protocols
    • Ability to demonstrate respect and professionalism for subjects' rights and individual needs

    LICENSES, CERTIFICATIONS, AND/OR REGISTRATIONS:
    Registered Dietitian (RDN/LDN) preferred but not required.


    EDUCATION:

    • Bachelor's degree required.
    • Dietetics/Nutrition training (preferred but not required).

    EXPERIENCE:

    • New graduates with some relevant course/project work or those without any prior research experience will be considered.
    • Experience with REDCap is preferred but not required.
    • Experience with nutrition support and/or sleep research.
    • Experience working with clinical populations (inpatient/outpatient).

    WORKING CONDITIONS:
    MGH research laboratory on main MGH campus, Boston. Primarily in-person, but hybrid flexible, if necessary. May be required to attend meetings outside of regularly scheduled hours.

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