• Clinical Research Manager - Lymphoma Service, Department of Medicine

    Job Locations USA-NY-New York
    Posted Date 2 weeks ago(4/11/2018 11:09 AM)
    Requisition ID
    2018-21373
    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

    The Lymphoma Service in the Department of Medicine (DoM), at MSK is seeking a Clinical Research Manager (CRM). The CRM serves as an integral member of the research team and oversees the daily operations and activities of the program including all therapeutic and biospecimen open and active studies, closed to accrual studies and pipeline studies.

     

    Job Duties include:

    • Staff Management: Supervise the training/development and performance management for at least 6 direct and at 30 indirect reports and responsible for the hiring of new staff.
    • Protocol Development: Work closely with the Protocol Activation Core in protocol development and oversees the operational aspects of opening new studies.
    • Financial Management: Works closely with the appropriate stakeholders, forecast trial resource needs, and assesses staffing resource needs for program and senior leadership to ensure appropriate line function allocations.
    • Clinical Trial Reporting: Generate protocol portfolio status reports for key stakeholders. Implements solutions for streamlining and accelerating the monitoring and review of clinical trials to significantly increase accrual to clinical trials, data cleaning, data quality, and trial completion.
    • Quality Assurance: participate in routine audits for data quality, regulatory compliance, patient safety issues related to clinical trial. Communicates and ensures compliance with company policies and procedures, quality standards and improvement initiatives.

    You need:

    • At Least 4 – 7 years of clinical research experience.
    • At least 2 years of direct staff management.
    • Thorough knowledge of Good Clinical Practice (GCP) guidelines, Human Subject Protection, clinical trial design, regulatory processes, and clinical development process required.
    • Therapeutic and Oncology Research experience strongly preferred.
    • Effective written/verbal communication and oral presentation skills required. Excellent interpersonal, leadership, decision-making and issue resolution skills are also required.

    #LI-PB1

    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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