Telemetry Monitor Technician​/CRA

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• Review protocols and comply with study-specific activities that impact telemetry areas of responsibility.
• Communicates in an appropriate and professional manner with study subjects and unit personnel.
• Maintain accurate and complete source data.
• Perform study protocol related activities, i.e., telemetry monitoring, etc., as assigned.
• Assist with telemetry monitoring system set‑up and preparation of telemetry transmitters and related documentation.
• Participate in continuous cardiac telemetry monitoring of study subjects, as required by the study protocols, and seek assistance as needed.
• Assist with telemetry data review in the telemetry monitoring system and generation of Holter reports, as appropriate.
• Maintain safety and confidentiality of study subjects throughout the study.
• Understands and complies with SOPs, FDA regulations, and basic GCP requirements.

• High School Diploma or equivalent.
• 1-2 years of work experience in a clinical or research environment; documented proficiency in Cardiac Arrhythmia recognition.
• Training schedule: 4-8 weeks, M-F 7:00 am–3:30 pm, depending on progress.
• Position primarily first‑shift weekdays, available weekends, occasional overnight shift after training completion. Training occurs on first shift.
• Requires face‑to‑face interactions with subjects and hands‑on skills involving physical contact (e.g., phlebotomy, ECG collections, vital signs).

• Cardiac Arrhythmia and phlebotomy.
• Lab work.
• Drawing blood.
• Taking vital signs.
• Clinical and/or hospital setting experience. Paramedics and firefighters do well in this position.

• Seniority level: Entry level
• Employment type: Contract
• Job function: Health Care Provider
• Industry: Pharmaceutical Manufacturing