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


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

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