MGR CLINICAL TRIALS OFFICE

    Moffitt Cancer Center
    Tampa, FL
    Full-time
    Similar jobs pay $26.38 - $52.89

    Job Description

    Manager of Clinical Trials Office

    Moffitt Cancer Center (MCC), an NCI-designated comprehensive cancer center in the state of Florida, and the #8 ranked Best Hospitals for Cancer on U.S. News & World Report, is seeking highly motivated individuals to join the Clinical Trials Office as Clinical Trial Managers. Be part of the significant contributions to the prevention and cure of cancer which is based on compassion for our patients, an emphasis on collaboration, and a culture of scientific excellence.

    Responsibilities:
    • Staff supervision and mentoring, monitor staff conduct, perform staff interviews, hire/terminations, and perform annual staff evaluations
    • Allocates staff based on acuity, staffing standards and expertise of personnel
    • Fiscal oversight: develop annual budget for the Clinical Trials Office cost center, review individual protocol budgets to assure adequate reimbursement; responsible for revenue creation, cost management and purchasing
    • Actively participate in operational review of new protocols and amendments for feasibility of conduct
    • Assist with development, revision and continuous evaluation of clinical research department standards and policies; participate in and/or lead process improvement working groups and staff mentoring education activities
    • Responsible for the direct supervisor of clinical research staff
    • Leads the daily clinical research operations for one or more key areas
    • Responsible for monitoring workloads and determining appropriate staffing levels for the clinical research staff (nurses, coordinators, and data specialists)
    • Works in collaboration with the Clinical Trials Business Office and Research Finance to coordinate budget development and research patient and sponsor billing
    • Responsible for budgeting and financial management of one or more cost centers
    • Takes the lead and/or participates in development and execution of training/mentoring programs, quality improvement processes and other projects, including the development of SOPs
    Credentials and Qualifications:
    • Bachelor's degree (Master's preferred)
    • Five (5) years of experience in executing multidisciplinary clinical research protocols (preferably in oncology)
    • Two (2) years of staff supervisory/management experience
    • Clinical Research certification (e.g. SOCRA, ACRP) preferred
    Moffitt offers excellent salary and benefits as well as Relocation assistance.

    Posting ID: 556732639Posted: 2020-05-22