Contract: Clinical Research Assistant / USA

Minimum Experience Required:

• 1-2 years of work experience in a clinical or research environment
• Documented proficiency in Cardiac Arrhythmia (must have experience) recognition (knowledge check will be included in the interview process)

Major Job 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.