Your Role As An Investigator

If you would like to conduct clinical research, CIS can offer the foregoing advantages and more by joining the CIS/MD Network at no cost to you.

• Perform timely quality research
• Identify suitable patients for enrollment in clinical trials
• Conduct clinical trials in accordance with Standard Operating Procedures
• Adhere to Good Clinical Practice
• Inform Clinical Investigation Specialists of potential competing studies

Our Commitment To You

As a collaborating member in the CIS/MD Network, CIS is committed to providing you with the tools necessary to perform quality clinical research. This includes the following four elements:

Centralized Marketing Program for Study Recruitment

• A dedicated marketing plan soliciting new studies on your behalf
• Contacts developed over a decade of experience in the pharmaceutical and biotechnology industries
• Exhibiting at major professional conventions and conferences
• Overall promotion of your site and staff as part of the CIS/MD Network

Staff Support and Quality Assurance

• Training as needed for clinical research coordinators
• Verification systems for data quality control
• Assist with meeting target enrollment goals

Regulatory Documentation

• Develop and assist with clinic guides for source documents
• Assist with regulatory documents (IRB forms, 1572's, CV's, etc.) as needed

Administration

• Assist with development of SOP's (Standard Operating Procedures)
• Obtain sponsor statements of indemnification
• Assist in patient recruitment if needed