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    Clinical Research Coordinator I - Los Angeles, United States - CEDARS-SINAI

    CEDARS-SINAI
    CEDARS-SINAI Los Angeles, United States

    Found in: CareerWallet US C2 - 4 days ago

    Cedars-Sinai background
    Full time
    Description

    Job Description

    Come join our team

    The Clinical Research Coordinator I works independently providing study coordination, screening of potential patients for protocol eligibility, presenting non-medical trial concepts and details, and participating in the informed consent process. Responsible for accurate and timely source documents, data collection, documentation, entry, and reporting including timely response to sponsor queries. Responsible for compiling and reporting on each study including information related to protocol activity, accrual data, workload, and other research information. Presents study information at regular research staff meetings. Ensures compliance with all federal and local agencies including the Food and Drug Administration (FDA) and local Institutional Review Board (IRB).

    Primary duties and responsibilities:

    • Independent study coordination including screening of potential patients for protocol eligibility, presenting non-medical trial concepts and details to the patients, and participating in the informed consent process.
    • Schedules patients for research visits and procedures.
    • In collaboration with the physician and other medical personnel, documents thoroughly on Case Report Forms (CRFs) the following; changes in patient condition, adverse events, concomitant medication use, protocol compliance, response to study drug.
    • Maintains accurate source documents related to all research procedures.
    • Responsible for accurate and timely data collection, documentation, entry, and reporting including timely response to sponsor queries.
    • Schedules and participates in monitoring and auditing activities.
    • Responsible for compiling and reporting on each study including information related to protocol activity, accrual data, workload, and other research information; present this information at regular research staff meetings.
    • Notifies direct supervisor about concerns regarding data quality and study conduct.
    • Works closely with a regulatory coordinator or directly with the Institutional Review Board (IRB) to submit Adverse Events, Serious Adverse Events, protocol deviations, and Safety Letters in accordance with local and federal guidelines.
    • May perform other regulatory / Institutional Review Board duties, budgeting duties, and assisting with patient research billing and reconciliation.
    • Ensures compliance with all federal and local agencies including the Food and Drug Administration (FDA) and local Institutional Review Board.
    • Maintains research practices using Good Clinical Practice (GCP) guidelines.
    • Maintains strict patient confidentiality according to HIPAA regulations and applicable law.
    • Participates in required training and education programs.

    Qualifications

    Educational Requirements:

    • High School Diploma/GED required
    • Bachelor's Degree in Science, Sociology or related degree preferred

    Licenses:

    • SOCRA or ACRP Certification preferred upon hire

    Experience:

    • One (1) year of clinical research related experience required

    About Us

    Cedars-Sinai is a leader in providing high-quality healthcare encompassing primary care, specialized medicine and research. Since 1902, Cedars-Sinai has evolved to meet the needs of one of the most diverse regions in the nation, setting standards in quality and innovative patient care, research, teaching and community service. Today, Cedars- Sinai is known for its national leadership in transforming healthcare for the benefit of patients. Cedars-Sinai impacts the future of healthcare by developing new approaches to treatment and educating tomorrow's health professionals. Additionally, Cedars-Sinai demonstrates a commitment to the community through programs that improve the health of its most vulnerable residents.

    About the Team

    Cedars-Sinai is one of the largest nonprofit academic medical centers in the U.S., with 886 licensed beds, 2,100 physicians, 2,800 nurses and thousands of other healthcare professionals and staff. Choose this if you want to work in a fast-paced environment that offers the highest level of care to people in the Los Angeles that need our care the most.
    Req ID : 1131
    Working Title : Clinical Research Coordinator I - Obstetrics & Gynecology - Accortt Lab (Full-Time)
    Department : Research - OBGYN
    Business Entity : Cedars-Sinai Medical Center
    Job Category : Academic / Research
    Job Specialty : Research Studies/ Clin Trial
    Overtime Status : NONEXEMPT
    Primary Shift : Day
    Shift Duration : 8 hour
    Base Pay : $ $39.76
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