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.
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.
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