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    Clinical Research Coordinator - Boston, United States - Partners Healthcare System

    Partners Healthcare System
    Partners Healthcare System Boston, United States

    2 weeks ago

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    Description

    GENERAL SUMMARY/ OVERVIEW STATEMENT:
    The focus of our research is on self-injury and depression among youth.

    We are currently looking to hire one full-time clinical research coordinator to assist with NIMH-and American Foundation for Suicide Prevention-funded studies aimed at improving short-term risk prediction for suicidal behavior in adolescents.

    Studies assessing proximal risk for suicidal behavior use computational methods to model neurocognitive markers and/or ambulatory indices (i.e., mobile technology including actigraphy, passive sensing of physiological arousal, passive sensing of social engagement and physical activity, and ecological momentary assessment) in psychiatrically hospitalized youth.

    Additional studies focus on employing computer vision to identify visual indicators of suicide risk among adolescents. Research coordinators will work under the mentorship of Dr. Richard Liu and Dr. Taylor Burke at Massachusetts General Hospital.

    These positions are particularly well suited for individuals seeking to gain research and clinical experience prior to graduate or medical school.


    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

    EDUCATION:

    • Bachelor's degree required.

    EXPERIENCE:

    • New graduates with some relevant course/project work or those without any prior research experience will be considered for the Clinical Research Coordinator position outlined above.

    SUPERVISORY RESPONSIBILITY (if applicable):

    • A Clinical Research Coordinator I does not have any supervisory responsibility.
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