Telemetry Monitor Technician/CRA

Responsibilities: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.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.