Site Monitoring and Management

Effective Clinical Trial Site Monitoring & Management

Proper site management is an essential element of clinical trial execution and in ensuring trial success.

Our site monitoring and management services include:

Monitoring of trial(s).
Source data verification partial or complete, as required.
Clinical research associate (CRA) as main contact person for Principal Investigator (PI) and study team.
Permanent interaction from site selection until closure of a site.
Ongoing quality control at the site.
Discussion of recruitment strategies with the study site.
Set up and maintenance of your trial master file and investigator site file.
Overview of patient recruitment progress and site performance.
Discussion of recruitment strategies.

“Thank you so much for all of your support on this program! We really appreciate the time and effort you have put in. The effort has been such a collaborative journey, and your expertise has been invaluable. We look forward to continuing our collaboration on our other studies with you.”

– QPS Client

“I wanted to say thank you to the QPS team for all of your hard work and efforts to complete the study analysis during what has been a very challenging year to date. You delivered the reports to the new agreed timeline and these were of a high quality.”

– QPS Client

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