Clinical Research Sleep Technologist (RPSGT/RST)

(Research Studies & Sleep Laboratory Operations) Department: Sleep Lab Reports To: Sleep Lab Manager / Research Coordinator Location: Rebis Clinic Location(s) Employment Type: Full-Time or PRN Schedule (FTE): Three 12-hour overnight shifts per week (7:00 PM – 7:00 AM). Schedule (PRN): As needed based on research activity and study enrollment; additional clinical sleep lab shifts may be required. Compensation: $32-$42/Hour Rebis is seeking a detail-oriented, technically skilled, and research-minded Sleep Technologist to support both clinical research and sleep laboratory operations. The Research Sleep Technologist serves as the primary technologist for research‑related sleep studies and data collection while maintaining competency in routine clinical sleep testing. This role is responsible for ensuring high‑quality physiologic data, participant safety, protocol compliance, and research integrity. Full‑time staff may also support regularly scheduled patient studies when research volume allows or operational needs require. This position is ideal for someone who enjoys combining patient care, technology, and scientific discovery to help advance the future of sleep medicine. About Rebis Rebis is a multidisciplinary sleep wellness center dedicated to transforming sleep health and restoring overall wellness. Our multidisciplinary model integrates sleep medicine, airway dentistry and functional medicine by implementing root cause diagnostics, and treatment pathways into a unified healing experience. Our mission is to restore and enhance individual healing by optimizing sleep health through a collaborative and multidisciplinary approach rooted in connection, integrity, and compassion. Our vision is to become the nation’s leading multidisciplinary center for sleep wellness, creating a comprehensive ecosystem of healing that empowers individuals to thrive. At the heart of Rebis is a simple commitment: Every person who interacts with us should feel Loved, Heard, and Safe. Why This Role Matters At Rebis, the Clinical Research Sleep Technologist helps bridge clinical care and scientific discovery. By executing research protocols with precision and collecting high‑quality physiologic data, this role contributes to innovations that improve diagnostics, treatments, and patient lives. While research studies are the primary focus, this position also supports clinical sleep laboratory operations to ensure high quality patient care and operational excellence. What You’ll Own Execute overnight research studies and participant monitoring. Ensure protocol compliance and research data integrity. Conduct research and clinical sleep studies with technical excellence. Support participant education and study completion. Maintain accurate documentation and audit‑ready records. Troubleshoot equipment and technical issues. Maintain research equipment and study readiness. Collaborate with research, clinical, and operational teams. Support routine sleep laboratory operations as needed. Our Operational Model Rebis operates on a patient‑centered, outcomes‑driven model rooted in precision diagnostics, hospitality, and collaborative care. Clinical Research Sleep Technologists are expected to combine technical excellence, protocol discipline, compassionate patient care, and operational accountability while consistently executing research protocols and sleep studies to the highest standards. Performance Expectations This is a quality‑driven and detail‑oriented role. Clinical Research Sleep Technologists are evaluated on: Protocol compliance Data quality and integrity Documentation accuracy Participant and patient experience Technical performance Operational reliability What Success Looks Like A successful Clinical Research Sleep Technologist at Rebis is a reliable, detail‑oriented technologist who executes research protocols with precision while maintaining exceptional participant care and data quality. They consistently: Execute research protocols accurately and consistently. Produce high‑quality physiologic data. Maintain excellent protocol compliance and documentation. Ensure participant and patient safety. Deliver an exceptional participant experience. Troubleshoot technical issues proactively and effectively. Support both research and clinical sleep studies with professionalism and reliability. Who Thrives in This Role We are looking for someone who: Has experience with pharmaceutical, academic or industry research. Enjoys combining patient care, technology, and research. Takes pride in accuracy and attention to detail. Is comfortable working independently and following structured protocols. Adapts well to changing priorities and study requirements. Values both scientific integrity and exceptional patient experiences. Core Responsibilities Research Operations Conduct research studies according to approved protocols. Support participant enrollment, education, and study completion. Maintain accurate documentation and research records. Ensure protocol compliance and data integrity. Clinical Sleep Testing Perform PSG, titration studies and other sleep testing as needed. Collect high‑quality physiologic data and troubleshoot technical issues. Ensure patient safety, comfort, and study quality. Operations & Collaboration Maintain equipment, supplies, and study readiness. Collaborate with research, clinical, and operational teams. Support quality initiatives and continuous improvement efforts. Required RPSGT or RRT‑SDS credential required Current BLS certification Previous clinical research experience Pediatric sleep experience Strong understanding of sleep physiology and AASM standards Strong technical troubleshooting skills Excellent organizational and documentation abilities Ability to work independently overnight Strong communication and critical thinking skills Preferred Experience working on industry‑sponsored studies Experience with device validation projects Experience with IRB‑regulated research Skills Sleep Technology Polysomnographic acquisition software proficiency (Compumedics preferred) PSG/MSLT/MWT protocol execution Research Methodology Good Clinical Practice (GCP) principles Protocol deviation identification and reporting Participant screening, enrollment, and informed consent execution Source documentation and audit trail maintenance Electronic data capture (EDC) platform proficiency Clinical Systems EHR/EMR documentation including charge capture and order reconciliation Study startup activities: site initiation readiness, delegation logs, training documentation Operational Medical equipment calibration and preventive maintenance logging Supply and inventory management across multi‑study environments Benefits Competitive compensation + Bonus eligibility Medical, dental, vision insurance 401(k) Unlimited PTO + paid holidays (FTE only) PTO to Celebrate of your 1st Breath (Birthday) Complimentary Rebis Within sleep care within Rebis PRN Benefits Flexible scheduling Supplemental income opportunities Exposure to innovative sleep medicine research Continuing education and training opportunities Join Rebis Rebis is building a high‑performance healthcare operating model focused on access, patient follow‑through, clinical outcomes, and excellent service. This is a strong opportunity for someone who wants to support cutting edge research opportunities to develop the future of sleep medicine care. #J-18808-Ljbffr S27a