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    Clinical Research Coordinator - Kansas City, United States - Insight Global

    Insight Global
    Insight Global Kansas City, United States

    3 weeks ago

    Insight Global background
    Description

    Job Description

    Job Description

    Position title: Sr. Clinical Research Coordinator

    Duration: 19 + months with extensions, can be on contract for up for 24 months

    Day to Day:

    This opportunity will be part of the clinical trials in a pharmacy. Bringing the trials to the people at their local pharmacy. The Senior Clinical Research Coordinator (CRC) is responsible for managing and overseeing the day-to-day operations of clinical trials, recruiting and screening study participants, as well as documenting and reporting on the daily operations of assigned trials. Working in collaboration with the Principal Investigator, the Sr. CRC is responsible for the oversight, facilitation and coordination of the daily clinical trial activities and plays a critical role in the conduct of the study. The Sr. CRC works collaboratively with the entire team, sponsors, and Clinical Quality Associates to ensure productivity, quality, and timely completion of studies. The Sr. CRC is expected to support, guide, train, demonstrate and lead clinical trial team members in the implementation of trial related activities. The Sr. CRC applies critical thinking and creative problem-solving skills across a wide variety of clinical studies, and contributes to the development of new processes, procedures, tools, and training to enhance clinical research activities and is accountable for adhering to quality standards

    Must Haves:

    • Willing to travel to a secondary site nearby to provide support or temporary coverage as needed
    • At least 3-5 years of experience as a Clinical Research Coordinator in the clinical trail space
    • Experience working on decentrailized/ hybrid clinical trails
    • Experience overseeing multiple clinical trials concurrently, while maintaining attention to detail
    • Working knowledge of ICH-GCP, US CFR, and HIPAA regulations
    • Has Phlebotomy certification

    Additional Details:

    • No OT allowed.
    • Potential to extend/ convert to FTE.
    • Hours of operation: M-F from 8am to 5pm. / Training will be the first week.
    Company Description· The work awarded is called Gulf Range Enhancement OTA. This OTA funds the company or testing efforts to enhance the Gulf Range. The Gulf Range is a land range 2-3x the size of Redstone. Testing ground for boats, planes, subsea product, etc. This team takes customer ideas makes it usable. They do all the mechanical, electrical, firmware, cyber, RF, networking, corrosion, obsolescence, integrations, fabrication, assembly, test. The customers who use the test range differ from who they are and what they want to test. Our team takes the want/idea, designs and develops a testable solution, and utilizes the repositories of techniques, tools, designs, etc. to continue to build our base solutions tool set. Because this is not one singular product and is a service to many potential products, the experience we are looking for needs to be multidisciplinary, general engineering services. Our team reprioritizes frequently.
    \t· They design/develops the solution all the way to the point of making it a testable product on the test range. One example that has just reached test phase is a 9x35 ft buoy out in the ocean that will serve as a launch pad for things. They will perform customer test support on it and are integrating into all their test operations.
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