Kennedy Krieger Institute

  • RESEARCH COORDINATOR - CLINICAL TRIALS UNIT

    Vacancy ID
    5122
    Pos. Category
    Research
    Job Location : Street
    1741 Ashland Ave
    # of Hours
    40.00
    Job Locations
    US-MD-Baltimore
    Pos. Type
    Regular Full Time
  • Overview

    the Research Coordinator in the Clinical Trials Unit assists and collaborates with the Principle Investigator (PI) and research collaborators to reach research goals.  This position requires a degree of responsibility, flexibility and independence to perform diverse duties including collecting, analyzing and archiving data.

    Responsibilities

    1. Prepare and submit Institutional Review Board (IRB) required materials, as well as prepare compliance and regulatory documentation for local, state, and federal agencies and any other pertinent entity.
    2. Assist and perform duties under the direction of the Senior Research Coordinators or the Manager of Medical Program Operations. Support daily clinical trial and research study activities including but not limited to (a) participant recruitment and scheduling, (b) study procedure scheduling and coordination, (c) obtaining results and ensuring clinician review, and (d) documentation completion.
    3. Communicate directly with research collaborators, study sponsor and study vendors.
    4. Manage research data in accordance with protocols established by sponsors and the Institute.
    5. Attend study and research related meetings, conferences, and teleconferences.
    6. Participate in research planning and development activities.
    7. Support Senior Research Coordinators or the Research Program Coordinator with data preparation, data entry, transfer, archiving, maintenance, and analysis. Provide and communicate data-related study progress, issues, and problems to research collaborators.   
    8. Assist with general administrative work including processing subject reimbursements and incentives, inventory and ordering supplies, and organizing service billing.
    9. Will work closely with the Manager of Medical Program Operations to develop and implement standard operating procedures.



    Qualifications

    EDUCATION:

    • Bachelor’s degree is required, preferably in psychology, statistics or neurosciences.

    EXPERIENCE:

    • Requires at least two (2) years of research related work experience.
    • Must be familiar with investigator initiated research projects and integrative research, including multi-site projects.
    • Must be proficient in data management using Microsoft Excel.

     

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