I2R has over 20 clinical development associates working on its behalf in the following disciplines:

• Clinical Trial Design
• Regulatory Affairs
• Site Monitoring
• Data Management
• Biostatistics
• Pharmacology
• Medical Writing
• Document Publishing

Additionally, I2R has consulting agreements with senior industry consultants, including ex-FDA staff, to assist with clinical and regulatory strategy, as well as content experts for IND development. This broad and in-depth clinical development knowledge across many disciplines coupled with strong, practical expertise, allows I2R to provide our clients with valuable and timely insight.

CVs are available upon request.