Site Selection

When high quality, experienced sites and investigators are selected to conduct your clinical trial you can expect high quality data. Our staff ensures that recruitment goals are met, the study protocol is executed properly and, that “first-in and last-out” milestones are met while yielding evaluable data. We understand that starting and ending every clinical trial on time is crucial to stay a step ahead of the competition.

Clinquest utilizes several approaches in identifying qualified investigators from our Clinical Trial Site Database. We consider the site’s location, staffing, qualifications, history, clinical trial experience, area of therapeutic experience, GCP/ICH compliance and patient population /enrollment history. Qualified clinical sites must continue to meet our very high standards to participate in future clinical research trials for our clients. We collaborate with you to select sites that will successfully meet your project needs.

We know that direct experience with a clinical site is the best predictor of future success. We offer you our experience in conducting over 100 clinical trials in the U.S, Canada, and Europe, and an established, impressive network of clinical trial sites with experienced investigators from Phase I – IV, across a variety of therapeutic areas.

Site Selection Core Services:

• Principal Investigator and Site Selection
• Feasibility Studies and Qualification
• Accelerated Site Regulatory Package (SRP) Services
• Clinical Trial Agreements (CTA)
• Site Contracts and Budget Preparation and Negotiation
• “Fast-track” Site Activation
• Informed Consent Form (ICF) Preparation and Review 
• Investigator Payments
• Insurance Agreements