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Clinical Research Associate (CRA) I
Clinical Research Associate (CRA) ISpectraforce Technologies • North Chicago, IL, United States
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Clinical Research Associate (CRA) I

Clinical Research Associate (CRA) I

Spectraforce Technologies • North Chicago, IL, United States
25 days ago
Job type
  • Full-time
Job description

Position Title : Telemetry Monitor Technician

Work Location : North Chicago, Illinois, USA, 60030

Assignment Duration : 1 Year (Possible Extension)

Work Schedule :
  • 100% onsite
  • Open 24 / 7, primarily PM weekdays
  • Available weekends and occasional overnight shifts for coverage after training
  • Training Schedule : 4-8 weeks, Monday-Friday, 7 : 00 AM - 3 : 30 PM, depending on progress
  • Position Summary

    The Telemetry Monitor Technician role involves face-to-face interactions with study subjects and hands-on skills for clinical research activities within the Clinical Pharmacology & Pharmacometrics Research Unit. The position focuses on continuous cardiac telemetry monitoring and related tasks to support clinical research protocols.

    Functional Area / Department

    Clinical Pharmacology & Pharmacometrics Research Unit

    Key Responsibilities

    • Review protocols and ensure compliance with study-specific activities impacting telemetry areas of responsibility.
    • Communicate professionally and appropriately with study subjects and unit personnel.
    • Maintain accurate and complete source data.
    • Perform study protocol-related activities, including telemetry monitoring, as assigned.
    • Assist with telemetry monitoring system setup and preparation of telemetry transmitters and related documentation.
    • Participate in continuous cardiac telemetry monitoring of study subjects as required by study protocols, seeking assistance as needed.
    • Assist with telemetry data review in the telemetry monitoring system and generate Holter reports as appropriate.
    • Maintain safety and confidentiality of study subjects throughout the study.
    • Understand and comply with Standard Operating Procedures (SOPs), FDA regulations, and basic Good Clinical Practice (GCP) requirements.
    • Qualifications & Experience

    • Minimum Education Required : High School Diploma or equivalent
    • Minimum Experience Required :

    • 1-2 years of work experience in a clinical or research environment
    • Documented proficiency in cardiac arrhythmia recognition (mandatory)
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    Clinical Research Associate • North Chicago, IL, United States

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