• CLINICAL RESEARCH 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
    5
    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

    Functional Responsibilities:

     

    • Coordinates with clinical staff to develop, implement and manage clinical research data files and materials.
    • Organizes and performs clinical research, utilizing internet and other available clinical resources.
    • Collects research data and prepares information for input and analysis.
    • Coordinates the development of forms and questionnaires.
    • Coordinates procedures to collect data from patient charts, medical records, interviews, questionnaires, and diagnostic tests. 
    • Monitors subject’s progress and reports adverse events.

     

     

     

    Qualifications

    Minimum/General Experience:

     

    1-2 years of experience in research or a related field. Demonstrates experience in data collection. Demonstrates experience with Microsoft Office (Word, Excel, etc.).

     

    Minimum Education:

     

    Associate’s degree in a related discipline. Two (2) years of specialized experience plus a High School diploma is equivalent to an Associate’s degree.

     

     

     

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