Site Support & Management

Insight-driven services to rapidly identify, initiate, and train the best-fit sites for your study.

Schedule Consultation

Set up your clinical study sites for success and speed your time to market

Some 80% of clinical studies run behind schedule, which can dramatically increase costs and decrease product competitiveness.

WCG’s Site Activation service gives you a suite of six solutions you can apply to dramatically accelerate clinical study start-up and completion globally, as well unburden your internal resources.

In nearly every case, these acceleration strategies also reduce complexity, lower costs, drive higher quality study results, and provide a faster path to enrollment.

3 days Site selection complete in three days with predictive analytics
50% increase in feasibility response rate
35% reduction in site contracting cycle time

Case Study

Merck identified sites for participation within three days. Previously, this process took eight to ten weeks.

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A best-in-class suite of services designed to speed study start-up, reduce cost, improve data quality, and ensure compliance

Best-Fit Sites

Site Selection

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.

Fast Initiation

Site Contracting

Our expert legal focus, plus our vast Knowledge Base™ of global contract terms and costs cuts your clinical trial negotiating cycles by up to 35%—plus reduce study costs.

Study Collaboration

Site Training

Launch fully-automated, 24/7 online site training solutions that significantly cut complexity, time and expense while ensuring full compliance.

Site Feasibility

Engage and assess the world’s most highly qualified clinical trial sites—and accomplish more than 25% faster.

Site Payments

We unburden sponsors and CROs from complex payment administration, while protecting data flow and preserving strong site relationships by ensuring timely, accurate site payments.

Document Exchange

Securely expedite your document flow and tracking to help clinical trials start faster and smoother—and create an impeccable audit record.

Only WCG provides a seamless, end-to-end path to accelerated site activation

meeting

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 Site Activation 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.

Site Activation Resources

Benchmark site performance for your study

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.