Senior Sleep Research Coordinator — Clinical Trials (Hybrid)

Myana; Minnesota; Hybrid; USD 119,832,000 - 128,142,000; Full time

Job summary

University of Minnesota seeks a lead Clinical Research Coordinator in Sleep Neurology to manage multiple sleep research studies under PI supervision. The role combines in-person visits 2–3 days weekly with remote coordination, ensuring GCP compliance, HIPAA data handling, and coordination with IRB and sponsors.

The coordinator will lead visits, consent participants, manage data, and liaise with clinical sites across the Twin Cities metro, supporting safety and protocol adherence.

Qualifications

• BA/BS in a health-related field plus at least four (4) years of work experience or advanced degree plus 2 years in research
• Experience with recruiting study participants and running research participant visits
• Ability to collaborate with clinical sites to conduct research visits
• Experience or interest in learning to complete remote participant visits

Responsibilities

• Lead clinical research study visits with participants in-person and remotely
• Identify, recruit, screen, and consent participants for sleep-related research
• Manage data entry from research visits with attention to detail
• Ensure HIPAA compliant secure data storage of all study materials
• Explain diagnostic and study procedures to participants
• Administer tests and route lab/clinical data to PI for evaluation
• Develop data collection methods and Case Report Forms (CRFs)
• Coordinate scheduling and communications with PI, sponsor, IRB, and participants
• Ensure compliance with GCP and SOPs across the study
• Coordinate site visits with sponsors and funding agencies
• Perform other duties as needed

Skills

Recruit study participants

IRB liaison

GCP compliance

Data entry and management

Education

BA/BS health-related field with 4+ years research

Advanced degree with 2+ years research experience

Job description

University of Minnesota seeks a lead Clinical Research Coordinator in Sleep Neurology to manage multiple sleep research studies under PI supervision. The role combines in-person visits 2–3 days weekly with remote coordination, ensuring GCP compliance, HIPAA data handling, and coordination with IRB and sponsors.

The coordinator will lead visits, consent participants, manage data, and liaise with clinical sites across the Twin Cities metro, supporting safety and protocol adherence.