• CLINICAL PROTOCOL COORDINATOR, STOPS

    Job Locations US-MD-Bethesda | US-AZ-Phoenix | US-MD-Rockville | US-MD-Bethesda | US-NC-Charleston | US-ND-Fargo | US-MD-Baltimore | US-NC-Charlotte
    # of Openings
    7
    Category
    Global Health
    Type
    Regular Full-Time
  • Overview

    CAMRIS International is an international development and research firm that realizes innovative solutions to health and development challenges through high-quality, cost-effective program and research management services. With experience working in more than 80 countries, we combine our proven systems with today’s most effective, evidence-based best practices to improve the lives of people around the world. We apply a customized, customer-centric, cost-effective business approach to offer greater value to our clients and challenge the way things have always been done in our field.

     

    CAMRIS clients include U.S. government agencies and multilateral and private organizations. Our core practice areas include public health, agriculture and food security, economic development, education, environment, humanitarian assistance, democracy and governance, and medical research. 

     

    CAMRIS is seeking exceptional candidates to provide scientific, technical, and other professional support services to assist the National Institutes of Health (NIH-- which is comprised of the Office of the Director and 27 Institutes and Centers) in meeting its operational objectives. Note: The positions are contigent on contract award.

    Responsibilities

    Coordinates with clinical staff to plan, implement, monitor and manage clinical protocols with Internal Review Board (IRB) requirements. Assists with protocol assembly, development and review of trial documents. Collaborates with clinical staff to develop and maintain trial related documents and operational procedures. Plans, implements, monitors and manages clinical protocols with IRB requirements. Reviews protocol data for entry in protocol database. Creates databases and coordinates data collection. Oversees the collection, distribution and filing of regulatory documents.

    Qualifications

    • 2-4 years of experience in a related field.
    • Expertise in the fundamentals of clinical trials.
    • Experience in clinical data management, database operations and analysis.
    • Familiarity with IRB requirements.

     

    Minimum Education:

     

    • Bachelors or Master’s degree in Life Sciences or other related discipline.
    • 1-2  years of specialized experience plus a BA/BS degree is equivalent to a Master’s degree.

     

     

     

    This effort is for a bid and contingent on award.

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