• Research Assistant

    Location US-NY-New York
    Posted Date 1 week ago(7/9/2018 7:57 AM)
    Job ID
    2018-10338
    Category
    Research & Academia - All Openings
    Emp Status
    Regular Full-Time
    Hours per Week
    35
    Shift
    Days
  • Overview

     

    The following statements are intended to describe the general nature and level of work being performed. They are not intended to be construed as an exhaustive list of all responsibilities, duties and skills required of personnel so classified.

     

    SUMMARY:

    This individual will be an integral member of the research team in compliance with all regulatory, institutional, and departmental requirements. The candidate will participate in all research study related activities and quality assurance of data for the projects assigned by the Principal Investigator.  The candidate will play an integral role in day-to-day research activities, patient coordination, and ensuring efficient operations. 

     

     

    RESPONSIBILITIES:

     

    Research

     

    Assist in the synchronization of research activities under the direction of the Principal Investigator of the research study and the Director of Clinical Research of the CJRC and serve as a liaison between the clinicians, research staff, and other research assistants.

     

    Provide overall administrative support for clinical research activities. Provides timely reports to the Institutional Review Board, the Principal Investigator, and sponsor(s) as needed.

     

    Contributes to research through recruitment process (conducts informed consent process), data collection, the development and build of Clinical Research Forms.

     

    Ensures that research is done in an accurate and efficient manner.

     

    Ensures that all research-related regulatory, institutional, and departmental compliance requirements are met as appropriate.

     

    Handles I.T. communications (requests) and generates reports from the registry as needed.

     

    Facilitates completion of all internal documentation needed for research (IRB applications, conflict of interest forms, data collection forms, etc.)

     

    Maintains and enhances professional growth through participation in seminars, research meetings, ARJR and CJRC grand rounds, and internal training sessions to keep abreast of trends in the field of Arthroplasty research.

     

    Assists in patient care coordination by assuring patients complete forms and patient reported outcomes prior to office visits.

     

    MINIMUM JOB REQUIREMENTS:

     

    Education/Training:    Bachelor’s degree required

     

    Experience:                

    • Prior research experience
    • Prior Epic experience
    • Prior hospital experience
    • Knowledge of Good Clinical Practice and Good Technology Practice
    • Excellent communication skills
    • Proficient use of computers and software
    • Knowledge of Orthopaedic and/or Rheumatologic terminology is a plus. 

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