• Clinical Trial Specialist - Multicenter Protocol Office

    Job Locations USA-NY-New York
    Posted Date 2 weeks ago(10/2/2018 9:30 AM)
    Requisition ID
    2018-24524
    Category
    Research - Clinical
  • Company Overview

    At Memorial Sloan Kettering (MSK), we’re not only changing the way we treat cancer, but also the way the world thinks about it. By working together and pushing forward with innovation and discovery, we’re driving excellence and improving outcomes.
     
    For the 28th year, MSK has been named a top hospital for cancer by U.S. News & World Report. We are proud to be on Becker’s Healthcare list as one of the 150 Great Places to Work in Healthcare in 2018, as well as one of Glassdoor’s Employees’ Choice Best Place to Work for 2018. We’re treating cancer, one patient at a time. Join us and make a difference every day.

    Job Description

    We are seeking a Multicenter Clinical Trial Specialist for our Multicenter Protocol Office.

     

    As a crucial member of the research team and in compliance with all regulatory, institutional, and departmental requirements, the Multicenter Clinical Trial Specialist will lead all efforts for the management of external sites to successfully participate in clinical trials led at MSK. This is a great opportunity in the growing arena of clinical research.

     

    You will:

    • Serve as the MSK point of contact for external sites in activities related to the clinical trial and maintain real-time knowledge of all aspects of the trial, including data management, subject management and regulatory oversight.
    • Perform diverse administrative and research-related duties requiring analysis, good judgment, comprehensive understanding of all federal regulatory standards and ICH (International Center for Harmonization) mentorship on Good Clinical Practice (GCP) and MSK CRA SOPs.
    • Ensure that participants are treated in accordance with the protocols.
    • Conduct real-time eligibility verification and risk-based monitoring (RBM) of external participants enrolled in MSK clinical trials.

    You are:

    • Capable of anticipating and stabilizing the needs of multiple partners.
    • Inventive, securing and deploying resources effectively and efficiently.
    • Adept at building partnerships and working reciprocally with others to meet shared objectives and goals.
    • Able to operate effectively, even when things are not clear or the way forward is not obvious.

    You need:

    • A High School Diploma/GED with 2-4 years of clinical research experience or equivalent required.
    • Bachelor’s degree preferred with experience in clinical research and/or other applicable research investigation. Relevant graduate work considered in lieu of minimum experience.

    Hours:

    • 9:00 a.m. – 5:00 p.m. (Monday-Friday)

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    Closing

    MSK is an equal opportunity and affirmative action employer committed to diversity and inclusion in all aspects of recruiting and employment. All qualified individuals are encouraged to apply and will receive consideration without regard to race, color, gender, gender identity or expression, sexual orientation, national origin, age, religion, creed, disability, veteran status or any other factor which cannot lawfully be used as a basis for an employment decision.  

     

    Federal law requires employers to provide reasonable accommodation to qualified individuals with disabilities. Please tell us if you require a reasonable accommodation to apply for a job or to perform your job. Examples of reasonable accommodation include making a change to the application process or work procedures, providing documents in an alternate format, using a sign language interpreter, or using specialized equipment.

     

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