Sleep Tech Research

About the role

Join a high-impact sleep research team and play a central role in bringing cutting-edge clinical/translational studies to life. In this position, you’ll coordinate study start-up and day-to-day execution of both industry and federally-funded sponsored sleep research—ensuring excellent data quality, participant safety, and full compliance with IRB and regulatory requirements. You’ll also have the opportunity to work closely with Dr. David Kent, advancing research that helps shape the future of sleep medicine.

Responsibilities

• Coordinate the approval processes and conduct of sleep research protocols from start-up through close-out
• Manage IRB/regulatory activities (submissions, amendments, continuing review, documentation)
• Conduct 1–3 overnight PSGs a month (varies with scheduling and research participants, allowing for a flexible schedule. YOU are in control of the schedule!)
• Ensure protocol adherence, accurate documentation, and high-quality data collection
• Partner with investigators, clinical staff, and research support teams to keep studies running smoothly and on timeline

Requirements

• Bachelor’s degree (or equivalent experience)
• 1 year of clinical research experience preferred
• RPSGT (Registered Polysomnographic Technologist) certification - a MUST
• Experience with Epic or other EHR

Benefits

• Monday–Friday schedule with flexibility (Mostly day shift!)
• Meaningful, hands-on work that directly supports research participants and scientific progress
• Close collaboration with a leading investigator in sleep research
• A role that blends clinical skill, coordination, and regulatory rigor—excellent for long-term growth in clinical research