Sponsor Services – 3@2x

Our team’s objective is to provide you with experienced, qualified clinical research sites for a successful and timely completion of a study.

We create well-established working relationships at each site and implement our Strategic Clinical Study Management Plan to ensure excellence and precision by conducting the following:

  • Engaging in routine communication with all of our sites.

  • Providing study update reports to our sites.

  • Reviewing enrollment goals and discuss recruitment strategies.

  • Scheduling regular meetings with both the CRC and Physician.

Our Sponsor Services Include:

site qualification@2x

Site Qualification Development

  • Pre-qualify sites to ensure study is a good fit and enrollment goals can be met
  • Site information packets provided to CRA
  • Site visit preparation (e.g. protocol and equipment review)
  • Site visit date and time coordination
document processing

Document Processing

  • Regulatory document completion within 7-10 business days
  • Centralized contract and budget negotiations within 7-10 business days
  • Central IRB submission


site management sponsor services

Site Management

  • Thorough up-to-date CV, licensure and training certification review
  • Standard Operating Procedures (SOP) binders
  • Patient recruitment marketing services
  • Identify process improvement areas and implementation

Our Sponsors: