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    Clinical Research Coordinator - Birmingham, United States - Medix

    Medix
    Medix Birmingham, United States

    2 weeks ago

    Default job background
    Engineering / Architecture
    Description

    Responsibilities

    • To collect and record preliminary data for clinical research programs
    • To recruit and perform follow-up with research participants as protocols outline
    • To schedule visits according to research protocols
    • To assist in coordination of lab and fieldwork
    • To maintain familiarity with appropriate Good Clinical Practice (GCP) guidelines and regulations
    • Prepares for study monitoring visits
    • Assists with correcting findings
    • Assists with the completion of Case Report Forms (CRF) according to protocol
    • Assists with development of protocols and standard operating procedures (SOPs) for data quality assurance
    • Performs general clerical duties (faxing, scanning, routing messages, coordinating the purchase of study supplies/materials)
    • May perform a variety of medical procedures under supervision
    • May assist in compiling, editing, and proofing written reports for both internal and external administrative offices
    • May perform data analysis using a variety of software packages
    • Uses Electronic Data Capture (EDC) systems necessary for operations under supervision
    • Performs other duties as assigned

    Key Duties & Responsibilities

    • Collects and records preliminary data for clinical research programs. Recruits and performs follow-up with research participants as protocols outline. Schedules visits according to research protocols.
    • Assists in coordination of lab and fieldwork. Prepares for study monitoring visits. Assists with correcting findings.
    • Assists with the completion of Case Report Forms (CRF) according to protocol.
    • Assists with development of protocols and standard operating procedures (SOPs) for data quality assurance.
    • Performs general clerical duties (faxing, scanning, routing messages, coordinating the purchase of study supplies/materials).
    • May perform a variety of medical procedures under supervision.
    • May assist in compiling, editing, and proofing written reports for both internal and external administrative offices. May perform data analysis using a variety of software packages.
    • Uses Electronic Data Capture (EDC) systems necessary for operations under supervision
    • Performs other duties as assigned.

    Qualifications

    • High School diploma or GED required
    • Prefer candidates with a bachelor's and two (2) years' experience working in a clinical setting
    • Knowledge of clinical trial processes, data collection, data entry
    • Experience with recruiting and performing follow-up with research participants as protocols outline
    • Knowledge of protocols and standard operating procedures (SOPs) for data quality assurance
    • Face-to-face patient communication experience
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