Qualifications:

High School Diploma required

CPR Certification required

Maintained RPSGT certification required

Prepare and calibrate equipment required for testing to determine proper functioning.

Apply electrodes and sensors according to accepted published standards.

Perform appropriate physiologic calibrations to ensure proper signals

Follow procedural protocols such as Multiple Sleep Latency Test (MSLT), Maintenance of Wakefulness Test (MWT), parasomnia studies, insomnia, etc. and to ensure collection of appropriate data.

Follow lights out procedures to establish and document baseline values such as bodies positions, oxyhemoglobin saturation, respiratory and heart rates.

Perform polysomnographic data acquisition while monitoring study-tracing quality to ensure signals are artifact-free. Identify and report signal abnormalities.

Document routine observations, including sleep stages and clinical events, changes in procedure and significant events in order to facilitate scoring and interpretation of polysomnographic results.

Score sleep/wake stages by applying professionally accepted guidelines.

Score clinical events such as respiratory events, cardiac events, limb movements and Arousals using center specific protocols.

Generate accurate reports by tabulating sleep/wake and clinical event data.

Maintain current CPR or BCLS certification.

Comply with the BRPT Standards of Conduct.

Responsibilities:

Promote safety and confidentiality of research participants at all times

Adhere to Occupational Safety and Health Administration (OSHA), Good Clinical Practices (GCP), Good Laboratory Practices (GLP), and infection control procedures

Plan and coordinate the initiation of research study protocol, and the implementation of operating policies and procedures

Plan, implement and maintain data collection and analysis systems in support of research protocol; may coordinate the collection and analysis of research data

Recruit, instruct and coordinate research subjects and/or volunteers, as appropriate to specific study objectives and work scope

Coordinate the day-to-day activities of technical support staff specifically engaged in the carrying out of research/clinical protocol, as appropriate to the position; may perform aspects of research protocol, as required, in accordance with specified program objectives

Organize and facilitate meetings, conferences, and other events associated with research activities; may perform and/or coordinate outreach activities, as appropriate to research objectives

Document all correspondence and communication pertinent to the research

Interact and communicate effectively with Principal Investigator, other site personnel, research participants, The Geneva Foundation, and the funding organization