Job Description

• 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.

• The new position would be pm weekdays and available weekends after completing training. Training would need to occur on 1st shift.
• This role requires face to face interactions with our subjects. It also requires hands on skills that require physical contact with some activities (ex: phlebotomy, ECG collections, vital signs).
• Name of Functional Area/Department: Clinical Pharmacology & Pharmacometrics Research Unit.
• Minimum Education Required: High School Diploma or equivalent.
• 1-2 years of work experience in a clinical or research environment; and Documented proficiency in Cardiac Arrhythmia (must have experience) recognition.

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