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

    Insight Global
    Insight Global Kansas City, United States

    1 week ago

    Insight Global background
    Healthcare
    Description

    Must-haves

    -Bachelor's Degree

    -At least 2 years' experience as a Clinical Research Coordinator

    -Experience working on decentralized/ hybrid clinical trails

    -Experience overseeing multiple clinical trials concurrently, while maintaining attention to detail

    -Experience working on clinical trails focusing on diabetes, obesity, and weight loss management

    -Working knowledge of ICH-GCP, US CFR, and HIPAA regulations

    -Phlebotomy certification

    Day-to-Day

    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.

    Manages and oversees the day-to-day operations in the administration of clinical trial activities at the site-level (i.e., direct interactions with study participants)

    Regularly interfaces with current and potential clinical trial participants to determine eligibility and consent of study participants in alignment with clinical trial protocol

    Creates standard operating procedures (SOPs) that adhere to all Food and Drug Administration (FDA) and Office for Human Research Protections (OHRP) regulations

    Contributes to the training of clinical trial staff and accountable for compliance with the operational requirements of the clinical trial

    Function as participants' primary point of contact, keeping them informed on the study progress, and facilitate involvement of other study team members, as needed (e.g., notify Principal Investigator of safety events)

    Manage participant visit scheduling and technical troubleshooting, escalating issues to the appropriate individual(s)

    Solicit and record information regarding safety events and preparing safety event documentation for review by the Principal Investigator

    Provides accurate and timely data collection, documentation, entry, and reporting in both Sponsor and client's databases

    Supports the regulatory staff in the maintenance of regulatory documents in accordance with the client's SOPs and applicable regulations

    Communicates and collaborates specific study requirements to the research team, including internal and external parties, sponsor, monitors, PI, and study participants

    Maintain regular contact with the Principal Investigator and team to review study details (e.g., progress, adverse events, enrollment)

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