Study Planning & Site Optimization
Insight-driven services to rapidly identify, initiate, and train the best-fit sites for your study.
Leverage leading-edge data, products, and services in the form of reports and on-line tools to inform your clinical development investment and operations strategy.
Engage and assess the world’s most highly qualified clinical trial sites—and accomplish more than 25% faster.
Launch fully-automated, 24/7 online site training solutions that significantly cut complexity, time and expense while ensuring full compliance.
Match your study’s therapeutic approach and protocols precisely to site and investigator performance track records, reducing site identification from the 8-10-week industry average to as quickly as three days.
Our research administration experts partner with your team to accelerate study start-up and ensure billing compliance.
Simplify the management of your entire clinical research portfolio by linking study status, patient enrollment, calendars, budgets, electronic data capture and more.
The WCG Site Feasibility Application drives efficient, site-friendly feasibility that results in faster study startup. The configurable application provides rapid development of clinical site surveys, more precise information results matched to your study, easier-to-answer surveys, and greater, faster cooperation from potential sites.
More importantly, this application permits close, step-by-step visibility of the entire qualification process, allowing you to manage and expedite it in real time.
The WCG Velos eResearch application is a robust clinical trial management system (CTMS) that automates administrative, financial, and research activities.
Velos eResearch simplifies the management of your entire clinical research portfolio by linking study status, patient enrollment, calendars, budgets, electronic data capture and more.
No other service provider offers sponsors and CROs a more focused or integrated portfolio of services dedicated to speeding clinical trial launches.
Our ability to speed site activation measurably—as well as reduce costs and improve the quality of study results—stems from our unmatched experience, proprietary Knowledge Base™ and highly-evolved technologies.
When you engage any of our Study Planning & Site Optimization services, you take advantage of our unmatched connections to all major sponsors and CROs. You also have access to our data on more than 36,000 (of about 40,000) FDA regulated PIs in the U.S., thousands of clinical trial contracts and budgets worldwide, and study performance on 2,700 research institutions in North America.
Interested to see how the investigators in your current or planned studies match up against the historic performance of all available investigators for the therapeutic area of the study?
Complete the form to schedule a consultation with WCG. We’ll share benchmark data from the WCG Knowledge Base, analyze your results, and share some of the common practices of top performers.