Senior Clinical Research Coordinator - Cerritos, United States - Oncology Institute, Inc.

    Oncology Institute, Inc.
    Oncology Institute, Inc. Cerritos, United States

    2 weeks ago

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    Description
    This is a fantastic opportunity to join our TOI Clinical Research team

    Description


    The Senior Clinical Research Coordinator conducts clinical research visits in accordance with ICH-GCP, TOI Clinical Research SOPs and sponsor protocols.

    Essential Duties and Responsibilities

    Understand clinical trial protocols (rationale, inclusion/exclusion criteria, study design, study medication and comparators, mechanism of action, required procedures, etc).


    Review detailed medical records including electronic medical records, lab reports, biopsies, radiology scans and other related medical data to confirm if a patient is eligible for a clinical trial.


    Liaise with other clinical research staff, medical providers and clinic staff to coordinate screening activities including but not limited to confirming patient eligibility, scheduling consents, placing screening orders to support patient randomization.

    Communicate individual patient and study level details with clinical trials sponsors, contract research organizations and other external providers.

    Document patient and study level activities in clinical trial management systems, tracking documentation and electronic medical records.

    Support management of regulatory documentation, investigational product storage and accountability as well as clinical data entry and query resolution

    Perform clinical trial visits with patients in partnership with clinic staff and providers in accordance with clinical trial protocols.

    Performs additional tasks as assigned by clinical research or clinic leadership.

    Responsible for overall conduct of assigned clinical research responsibilities.


    Education and Experience:
    Bachelor's degree in life sciences or equivalent combination of other degrees or certifications (nursing, phlebotomy, medical assistant, etc) and experience

    4+ years of clinical research experience


    Skills:
    In-depth knowledge of clinical research and ICH-GCP guidelines

    Proficient in Microsoft Office, Outlook, and other computer use

    Ability to organize a high-volume workload and prioritize tasks accordingly

    Strong work ethic, personal integrity, focus on collaboration, timeliness and dependability

    Bilingual in English and Spanish preferred, not required

    Schedule and Location:

    8 Hour Day Shift, Monday to Friday

    Local travel between corporate headquarters and treatment clinics

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