• SENIOR CLINICAL RESEARCH COORDINATOR

    Job Locations US-MT-Hamilton
    # of Openings
    3
    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 Senior 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.

    Responsibilities

    Duties Include: 

    • Coordinates with clinical staff to independently develop, implement and manage clinical research data files and materials.

    • Assembles, develops and reviews new research projects.

    • Provides assistance to staff in the collection, development and quality control of essential clinical research efforts.

    • Collects research data, prepares information for input and analysis and prepares reports.

    • Assists in the creation/ management of clinical website.

    • Develops/maintains research protocols, and educates staff.

    • Provides training to new research coordinators.

    • Works with outside company and CRAs that provide on-site monitoring.

    • 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 Education

    • Ph.D. in a related discipline desired. Three (3) years of specialized experience plus a Master’s degree is equivalent to a Ph.D. Five (5) years of specialized experience plus a Bachelor’s degree is equivalent to a Ph.D.

       Minimum Experience:

    • 3-7 years of experience in clinical research or a related field.

    • Demonstrates superior experience with data collection.

    • Demonstrates expertise with Microsoft Office (Word, Excel, etc.).

    • Demonstrates superior knowledge of research protocols and clinical, scientific and/or medical terminology.

     

     

     

     

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