Sponsors & CROs

Start up time is critical to the success of a clinical trial as delays translate directly into lost revenue. Sponsors benefit from experienced sites and efficient management of trials. PharmaSeek’s ability to quickly identify high-performing sites for Sponsors allows a clinical trial to begin without delay. We evaluate the history of a site and the background of its investigative staff before proposing it as an option to the Sponsor or CRO. Our facilitation of rapid site activation saves time and reduces costs.

Once we become involved in a project, we assign a project manager as a single point of contact for the Sponsor, CRO, and investigative sites. The project manager facilitates efficient communication, allowing PharmaSeek to keep the clinical trial moving forward at all times. Additional value to Sponsors and CROs accrue from the use of one contract template and budget for multiple sites.

Our network of approximately 250 investigative sites supports all major therapeutic areas and geographic regions of North America. PharmaSeek maintains a personal relationship with each site, allowing our team to quickly match clinical studies with qualified sites.

PharmaSeek does not have exclusive relationships with our investigative sites. Unlike a broker that charges fees before the work begins, we only receive compensation if the site successfully enrolls subjects into the study.  As such, our financial interests are completely aligned with the Sponsor and CRO.

For more information please contact Lisa Marks at or (866) 928-3339 Ext. 2.