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    Coordinator, Clinical Trials II-Center for Health Research - Portland, United States - Kaiser Permanente

    Kaiser Permanente
    Kaiser Permanente Portland, United States

    19 hours ago

    Kaiser Permanente background
    Description

    Job Title: Clinical Trial Research Coordinator II

    Company: An exciting opportunity with a leading healthcare organization based in Portland, OR is now available for a Clinical Trial Research Coordinator II (CTRC-II). This position offers a hybrid work setup, allowing you to work both onsite and remotely.

    The CTRC-II plays a crucial role in coordinating and overseeing clinical trial research projects. This hands-on position involves working closely with key stakeholders such as Project Managers, Clinical Trial Nurses, and Investigators to ensure the smooth execution of clinical trials while upholding the highest standards of ethical conduct.


    Essential Responsibilities:
    • Support and comply with organizational guidelines, procedures, and regulations related to clinical trials.
    • Maintain confidentiality and security of participant data.
    • Collect and document research data accurately and in a timely manner.
    • Coordinate participant assessments and study visits efficiently.
    • Assist in protocol compliance and data submission to sponsors.
    • Coordinate specimen handling and shipping according to regulations.
    • Support long-term data collection efforts for study participants.
    • Assist in participant recruitment and consent processes.
    • Contribute to drug accountability coordination and maintenance.
    • Facilitate study closure activities and documentation.
    • Communicate effectively with internal and external stakeholders.
    • Contribute to quality assurance and training initiatives.
    • Adhere to departmental policies for research integrity and compliance.
    • Participate in training and development activities for professional growth.
    • Perform quality control activities and support improvement initiatives.
    • Handle IRB documentation and communications as required.
    • Other duties as assigned.
    Basic Qualifications:
    • Minimum one (1) year of clinical trials research experience OR a bachelor's degree.
    Education:
    • Associate's degree or higher OR two (2) years of related field experience.
    • High School Diploma or GED required.
    License, Certification, Registration:
    • Basic Life Support certification required within 3 months of hire.


    Additional Requirements:
    • Must be proficient i


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