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    Clinical Research Coordinator - Memphis, United States - One GI®

    One GI®
    One GI® Memphis, United States

    2 weeks ago

    Default job background
    Healthcare
    Description

    Have you been looking for a place to grow your skillset? Or perhaps you are looking for a place to develop your career surrounded by a diverse group where employees feel a sense of belonging.

    At Gastro One we are championing the power of inclusivity and a people first mentality. We hope to improve the human experience – from our patients to our colleagues.

    If you are interested in joining our culture, we're looking for a Clinical Research Coordinator.

    The Perks

    • 401k with match
    • Tuition reimbursement
    • Competitive health & supplemental benefits
    • Excellent paid time off for balance of work/life.
    • Internal growth opportunities with training and development.

    Snapshot of Daily Duties

    • Administratively and clinically manage industry sponsored clinical trials.
    • Assist in patient recruitment by performing detailed chart reviews and patient interviews
    • Discuss study protocols with patients and verify the informed consent documentation.
    • Review medical history of patient against inclusion/exclusion criteria of studies.
    • Perform blood draws, process and ship blood/urine specimens per study protocol and IATA regulations.
    • Schedule all patient research visits and procedures consistent with protocol requirements
    • Dispense study medication, collect vital signs, and perform ECGs.
    • Complete and maintain case report forms per FDA guidelines and review them against the patient's medical record for completeness and accuracy.
    • Monitor patients and providing information to the medical staff and other staff members to assure optimal outcomes.
    • Coordinate the availability and distribution of medications for patients in a timely manner.
    • Responsible for the education of patients in all aspects of the disease process and/or clinical study in which the patient may be involved.
    • Assist the principal investigator and research director with various administrative tasks associated with the day-to-day operations of research studies and projects.
    • Facilitate assigned clinical trial from start to finish.

    The Must Haves

    • Associate Degree in a clinical or scientific related discipline required. Bachelors preferred
    • One (1) year previous experience as a clinical research coordinator for pharmaceutical phase II or III trials required.
    • Clinical experience in an office or hospital setting.
    • Research experience or equivalent.
    • BLS certified.
    • Understanding of Code of Federal Regulations for Human Subjects.
    • Certified in GCP's and HSP.
    • Phlebotomy experience preferred.
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