IRB & Regulatory Specialist I - Clinical Trials (Hybrid)

University of Kentucky; Lexington (KY); Hybrid; USD 32,000 - 53,000; Full time

Job summary

University of Kentucky is recruiting a Research Regulatory Specialist I to support IRB operations, regulatory documentation, and compliance for clinical trials. The role emphasizes handling IRB processes, HIPAA training, and data organization within a hybrid work setting.

The position requires a BS and at least one year of related experience, with duties including coordination of regulatory activities and support for research teams at the Markey Cancer Center.

Qualifications

• Bachelors degree and at least one year of related experience or UK equivalencies.

Responsibilities

• Assist with IRB applications and renewals across UK and other cancer centers.
• Manage regulatory documents and maintain project listings.
• Coordinate reports and submissions for regulatory agencies and internal review boards.

Education

BS

Job description

University of Kentucky is recruiting a Research Regulatory Specialist I to support IRB operations, regulatory documentation, and compliance for clinical trials. The role emphasizes handling IRB processes, HIPAA training, and data organization within a hybrid work setting.

The position requires a BS and at least one year of related experience, with duties including coordination of regulatory activities and support for research teams at the Markey Cancer Center.