Hybrid Clinical Research Regulatory Specialist I Neurology

University of Cincinnati; Cincinnati (OH); Hybrid; USD 55,000 - 75,000; Full time

Benefits offered by this job

Tuition remission

Comprehensive health coverage

Robust retirement plans

Paid time off

Parental leave

Professional development

Job summary

The University of Cincinnati College of Medicine seeks a full-time Clinical Research Regulatory Specialist I to coordinate regulatory activities for clinical research. The role involves reviewing documents, ensuring compliance with regulatory frameworks, and liaising with IRBs, sponsors, and contracting offices.

The position offers a hybrid work arrangement near the main campus in Clifton, Ohio. Required is a Bachelor's Degree and 1-2 years of relevant experience.

Qualifications

• Bachelor's degree required.
• 1-2 years of relevant experience.
• Experience coordinating regulatory activities preferred.

Responsibilities

• Prepare and submit protocol-specific documentation to IRBs and regulators.
• Serve as liaison for designated research protocols and stakeholders.
• Interpret and apply federal, state, and local regulations to ensure ethical research practices.
• Maintain regulatory documentation within systems (e.g., Complion).
• Assist with development and execution of research agreements.
• Coordinate site visits and communicate with sponsors/CROs.

Skills

Regulatory submissions

IRB liaison

Documentation management

Sponsor communications

Education

Bachelor's Degree

Tools

Complion

Job description

The University of Cincinnati College of Medicine seeks a full-time Clinical Research Regulatory Specialist I to coordinate regulatory activities for clinical research. The role involves reviewing documents, ensuring compliance with regulatory frameworks, and liaising with IRBs, sponsors, and contracting offices.

The position offers a hybrid work arrangement near the main campus in Clifton, Ohio. Required is a Bachelor's Degree and 1-2 years of relevant experience.