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    Clinical Research Coordinator - Los Angeles, United States - Medix™

    Default job background
    Engineering / Architecture
    Description

    Are you a CRC with 2+ years of experience and are wanting to gain CRO experience? This is the PERFECT opportunity for you

    Must Haves:

    • BS/BA in life sciences or educational equivalent and/or relevant work experience in a clinical environment or medical setting
    • Minimum 2 years as a Clinical Research Coordinator

    Important Details:

    • 100% ON SITE
    • Up to 18 hours per week, open to candidate preferences but NO weekends or evenings, must be during business hours

    Description:

    Clinical Research Coordinators (CRC) perform protocol specific duties relevant to the clinical trial in a defined scope that assists the site with patient recruitment.

    Scope of Support:

    • Administrative Support customized site level support, such as support with regulatory document submissions and perform chart reviews/EMR interrogation
    • Prescreening including review of concomitant meds, medical history, and inclusion/exclusion criteria to identify potential patients
    • Scheduling Visits including appointment reminders
    • Data Entry and Query Resolution based on data available in source documents and ensure data entry and responses are completed within protocol designated windows
    • External Referral Outreach including grassroots effort to distribute study recruitment materials in and around sites, community outreach
    • Contact, prescreen, and schedule referrals from outreach campaign
    • Conduct Study Visits
    • Perform ICF process following GCP

    Qualifications and Functions for this Role:

    • BS/BA in life sciences or educational equivalent and/or relevant work experience in a clinical environment or medical setting
    • Minimum 3 years in Clinical Research and preference for relevant healthcare experience
    • Certification of CCRC or CCRP preferred
    • Experience of EDC entry and query resolution preferred
    • Knowledge of clinical trials, combined with in-depth knowledge of departmental, protocol and study-specific operating procedures, consent forms, and study schedules
    • Comprehensive knowledge of GCP and ICH guidelines
    • Excellent interpersonal skills with the ability to establish and maintain effective working relationships with co-workers, managers and clients
    • Preference for Phlebotomy Certification


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