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    Clinical Research Coordinator - Pearland, United States - ICONMA

    ICONMA background
    Description
    Clinical Research Coordinator

    • Location: Pearland, TX
    • Duration: 12 months

    Description:
    - Knowledge of ICH-GCP, US CFR, and HIPAA regulations
    - Experience overseeing multiple clinical trials concurrently with attention to detail
    - Task prioritization and resource management to meet deadlines
    - Proficiency in phlebotomy and experience in decentralized/hybrid clinical trials


    Responsibilities:
    - Manage clinical research studies according to standard operating procedures
    - Interact with clinical trial participants to determine eligibility and consent
    - Coordinate research participant visits and procedures in adherence to protocols and schedules
    - Maintain communication with participants, informing them of study progress and involving other team members as necessary
    - Record safety events and prepare documentation for review
    - Ensure data integrity and record source data accurately
    - Support regulatory staff in document maintenance
    - Communicate study requirements to the research team and external parties
    - Maintain contact with the Principal Investigator to review study details
    - Manage study supplies and participant stipends
    - Conduct research study visits and procedures as per protocol
    - Respond promptly to queries and document study-related issues
    - Disburse investigational product, manage inventory, and provide patient education
    - Monitor site compliance with safety reporting and enhance subject safety


    ICONMA is an equal opportunity employer, fostering an inclusive employment environment regardless of race, color, religion, age, sex, national origin, disability, genetics, veteran status, sexual orientation, gender identity, or any other characteristic protected by law.



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