SCI Clinical Trials Office

SCI-CTO provides central coordination and oversight of clinical staff to ensure consistent processes, regulatory compliance, and improved efficiencies.

SCI-CTO provides a centralized resource that assists clinical researchers with scientific review, regulatory management, pre-award financial management, quality assurance, training and education, data collection, and monitoring.

SCI-CTO provides staff orientation training and ongoing education, supports investigator training, and manages the development and maintenance of Standard Operating Procedures (SOPs), Practice Guidelines, and study management tools.

Quality control monitoring of SCI clinical trials are conducted by SCI-CTO quality monitors or third-party monitors. Our external quality monitoring visits are primarily conducted remotely.

SCI-CTO MedLink Guidelines

Monitor Handout Document

SCI-CTO Monitor Memo

The SCI oversees the conduct of research studies investigated by SCI investigators, ensuring the research is of scientific merit, high quality, reliable, and verifiable.