Our project managers have extensive experience in conducting clinical trials. They serve as a central contact point to facilitate CRO/sponsor and site interaction. Our project managers have extensive CRC experience and are dedicated to patient recruitment and retention for individual sites. They manage all aspects of the clinical trial form study initiation to closeout.

As part of its documentation service SibPharma offers:

• Completion of regulatory documentation, including IRB submission as well as early approvals
• Preperation of source documents for each study
• Maintaining file storage