Katalyst CRO
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
High School Diploma or equivalent. 1-2 years of work experience in a clinical or research environment; and Documented proficiency in Cardiac Arrhythmia recognition. The training schedule is 4-8 weeks, M-F 7a-3:30p, depending on progress. The new position would be primarily pm weekdays, available weekends, and an occasional overnight shift for coverage 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). Top Skills
Cardiac Arrhythmia and phlebotomy. Lab work. drawing blood. taking Vital signs. clinical and/or hospital setting. Paramedic and firefighters do well in this position. Seniority level
Entry level Employment type
Contract Job function
Health Care Provider Industries
Pharmaceutical Manufacturing
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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. Requirements
High School Diploma or equivalent. 1-2 years of work experience in a clinical or research environment; and Documented proficiency in Cardiac Arrhythmia recognition. The training schedule is 4-8 weeks, M-F 7a-3:30p, depending on progress. The new position would be primarily pm weekdays, available weekends, and an occasional overnight shift for coverage 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). Top Skills
Cardiac Arrhythmia and phlebotomy. Lab work. drawing blood. taking Vital signs. clinical and/or hospital setting. Paramedic and firefighters do well in this position. Seniority level
Entry level Employment type
Contract Job function
Health Care Provider Industries
Pharmaceutical Manufacturing
#J-18808-Ljbffr