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Site Optimization Solutions
Drive clinical study site success and speed your time to market.
Enable smarter, faster, and more efficient research sites.
Improve communication with sites and reduce their administrative burden with WCG’s site optimization services. WCG makes it easy for sites and sponsors with fast activation and start-up, enhanced study conduct, transparent communications, regulatory compliance, staff augmentation services and timely site training – either in-person or virtual.
To improve the study start-up timelines and financial performance of sites, WCG also offers billing compliance, contract, and budget services to keep your studies on track, and financial management services to identify uncollected revenue.
Reduce overall study start-up timelines by as much as 35%
Cut site training costs by 50%
Engage the world’s most qualified clinical trial sites, and complete feasibility more than 25% faster
Explore Site Optimization Solutions:
Solutions for Research Sites
Study Start-Up
Shorten your study start-up timelines, ensure billing compliance, and enroll patients sooner.
Research Professionals
Optimize your existing site resources with flexible and scalable research professional support.
Financial Management
Implement better processes and consistent methods to build a financially healthy research program.
Study Advertising
Increase patient enrollment for your clinical trials through personalized, study-specific advertising campaigns.
Site CTMS
Simplify the management of your entire clinical research portfolio by linking study status, patient enrollment, calendars, budgets, electronic data capture and more.
Research Management
Streamline the IRB process, reduce costs, eliminate research errors, and improve process transparency and data reporting.
Solutions for Sponsors
Site Feasibility
Engage and assess the world’s most highly qualified clinical trial sites—and accomplish more than 25% faster.
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.
Clinical Trial Training
Launch fully-automated, 24/7 online site training solutions that significantly cut complexity, time and expense while ensuring full compliance.
Total Safety Solution
Relieve the burden of managing global drug safety and safety reporting operations with our end-to-end safety solution.
Meet the technologies that power our Site Optimization solutions
Investigator Space
Manage investigator training and safety reporting across all your sites and studies–with one login.
eResearch CTMS
Automate administrative, financial, and research activities with this robust clinical trial management system.
Related resources:
Blog Post
Video
Harnessing the Power of Data to Optimize Site Selection for Clinical Trials
Read More about Harnessing the Power of Data to Optimize Site Selection for Clinical Trials
Video
Better Together: How to Strengthen Sponsor and Site Partnerships – A Panel Discussion
Read More about Better Together: How to Strengthen Sponsor and Site Partnerships – A Panel DiscussionOptimize your site performance
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