• Clinical Protocol Coordinator

    Posted Date 2 months ago(8/22/2018 8:33 AM)
    Job ID
    2018-3137
    # of Openings
    1
    Job Location(s)
    US-MD-Bethesda
    Category
    Research
  • Overview

    Medical Science & Computing (MSC) is an exciting growth oriented company, dedicated to providing mission critical scientific and technical services to the Federal Government. We have a distinguished history of supporting the National Institutes of Health (NIH) and other government agencies. MSC offers a dynamic and upbeat work environment, excellent benefits and career growth opportunities.

     

    We attract the best people in the business with our competitive benefits package that includes medical, dental and vision coverage, 401k plan with employer contribution, paid holidays, vacation, Medical and Flexible Spending Accounts, Pre-Tax Transit Assistance and tuition reimbursement. If you enjoy being a part of a high performing, professional service and technology focused organization, please apply today!

     

    Duties & Responsibilities

    Medical Science & Computing is searching for a highly motivated Clinical Protocol Coordinator to support the National Institutes of Health (NIH). This opportunity is a full-time position with MSC and is on-site in Bethesda, MD.

     

    Duties and Responsibilities:

     

        • Oversee operations and project timelines on large, complex studies.
        • Responsible for evaluation and mitigation of risks to data and process across program.
        • Oversees process design and management.  Develops workflows and best practices for genomic research program that returns clinical results to participants.
        • Perform core data management functions including case report form documentation, edit check development, data cleaning.
        • Coordinate and perform responsibilities related to research participants including determining subject population availability, developing informed consents and screening materials, screening and recruiting subjects, scheduling visits, obtaining informed consent, overseeing study visits, and providing support to the result reporting process.
        • Contribute to the design, methodology, implementation, and regulatory review of research protocols, including management of manual of operating procedures.
        • Supervise and coordinate the collection, processing, shipment and storage of biospecimens.
        • Contribute to developing educational materials and educating colleagues about genomic research studies and related issues.

     

    Requirements

    Position Requirements:

     

    • Masters degree in a related field such as public health, nursing, genetics, or genetic counseling is required with at least 2+ years of related professional experience.
    • Project management experience is required.
    • Working knowledge of GCP and Human Research Subjects Protection guidelines, as well as regulatory requirements relating to clinical development and compliance with safety, ethical, legal and regulatory standards preferred
    • Demonstrated current understanding of the regulations as they relate to clinical trial data management systems and activities; demonstrated current understanding of Good Clinical Data Management Practices (GCDMP). Be detail oriented, able to work independently and efficiently to track multiple deadlines and keep projects on target and moving forward.
    • Able to anticipate and identify problems, consider alternatives, and work collaboratively and creatively to solve problems.
    • Familiar with statistical packages and Microsoft Office software, including email, word processing, spreadsheets, and presentations.
    • NIH credentialed/NIH experience highly desirable.

     

    Medical Science & Computing is an Equal Opportunity/Affirmative Action employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability, or protected Veteran status.

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