• CLINICAL RESEARCH COORDINATOR

    Job Locations US-MT-Hamilton
    # of Openings
    16
    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 for the Clinical Research Coordinator positions. S/he will support the mission of The National Institute of Allergy and Infectious Diseases (NIAID) and The National Institutes of Health (NIH) by conducting and supporting basic, translational and clinical research to better understand, treat, and ultimately prevent infectious, immunologic, and allergic diseases at the Rocky Mountain Laboratories in Hamilton, Montana.

     

    *This is a forecasted position and it is contingent upon contract award. 

    Responsibilities

    For Entry Level to Mid Level Roles, Duties Include: 

    • Coordinate with clinical staff to develop, implement and manage clinical research data files and materials.
    • Organize and perform clinical research, utilizing internet and other available clinical resources.
    • Collect research data and prepares information for input and analysis.
    • Coordinate the development of forms and questionnaires.
    • Coordinate procedures to collect data from patient charts, medical records, interviews, questionnaires, and diagnostic tests. 
    • Monitor subject’s progress and report adverse events.

    For Senior Roles, Duties Include:

    • Coordinate with clinical staff to develop, implement and manage clinical research data files and materials.
    • Organize and perform clinical research, utilizing internet and other available clinical resources.
    • Collect research data and prepares information for input and analysis.
    • Coordinate the development of forms and questionnaires.
    • Coordinate procedures to collect data from patient charts, medical records, interviews, questionnaires, and diagnostic tests. 
    • Monitor subject’s progress and report adverse events.
    • Oversees assurance of adherence to SOPs, good clinical practice, and FDA regulations.

     

     

    Qualifications

    For Entry Level Roles:

     

      Minimum Education

    • Associate’s degree in a related discipline. 

        Minimum Experience

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

    For Junior Roles: 

     

      Minimum Education:

    • Bachelor’s degree in a related discipline. 

       Minimum Experience: 

    • 2-5+ years of experience in a related field.
    • Demonstrate experience in data collection.
    • Demonstrate experience with Microsoft Office (Word, Excel, etc.).
    • Demonstrate knowledge of research protocols.

    For Mid Level Roles:    

     

        Minimum Education:

    • Master’s degree in a science related field is required.

        Minimum Experience:

    • 5-10+ years of experience in a clinical research or a related field.
    • Demonstrates strong experience with data collection.
    • Demonstrates experience with Microsoft Office (Word, Excel, etc.).
    • Demonstrates advanced knowledge of research protocols and clinical, scientific and/or medical terminology.

     For Senior Roles:

     

      Minimum Education:

    • Ph.D. in a science related field is required.

      Minimum Experience:

    • 10-15+ years of experience in a clinical research or a related field.
    • Demonstrates strong experience with data collection.
    • Demonstrates experience with Microsoft Office (Word, Excel, etc.).
    • Demonstrates advanced knowledge of research protocols and clinical, scientific and/or medical terminology.

     

     

     

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