Site Enablement for Sponsors & CROs

Connecting sponsors and CROs with advanced solutions to help optimize their study sites for faster clinical trials.

Accelerate your trials and reach your study endpoints faster with our site enablement solutions.

Complex protocols, increased demands for data collection, and ongoing pressure to achieve study endpoints faster are putting increased burdens on clinical trial teams. Each trial has its own concerns, and understanding each study’s unique characteristics is critical to identifying the areas that commonly contribute to study delays.

To enable studies to reach endpoints faster, WCG offers a set of comprehensive and integrated solutions to accelerate research activities at sites and conduct your trials more efficiently. Powered by advanced technology, scientific and operational expertise, and our proprietary healthcare data set, WCG Data Intelligence, our Site Enablement solutions are designed to identify study bottlenecks, activate sites faster, and accelerate enrollment.

For starting and conducting your studies as efficiently as possible, WCG offers

WCG Site Network

Partner with a network of over 470 clinical research site locations and 1,000+ PIs ready to conduct and accelerate your trials in virtually every therapeutic area.

Participant Identification

Optimize internal and external referral sources to efficiently identify participants that meet your study’s criteria.​

Participant Enrollment

Enroll identified participants through a streamlined engagement process.​

Participant Retention

Ensure strong retention rates through regular engagement with enrolled study participants.

Documentation Support

Ensure study data is effectively reviewed, collected, entered, and verified within your study’s timeline.​

Clinical Trial Training

Simplify the training experience for study teams and sites with live face-to-face, virtual, on-demand, and SIV meeting delivery with WCG InvestigatorSpace®.  

Safety Letter Acknowledgement

Manage critical and regulatory-required patient safety notifications to Principal Investigators through WCG InvestigatorSpace®. 

Rater Qualification and Training

Provide standardized endpoint training to raters, ranging from minimal to highly experienced, for accurate, consistent, and objective endpoint outcomes with WCG InvestigatorSpace®. 

Regulatory Document Exchange

Get a seamless experience to exchange critical study information with WCG InvestigatorSpace® through best-in-class workflows and CTMS and eTMF system integration capabilities. 

Technologies that support the success of your studies and sites

Accelerate your trials and reach your study endpoints faster.

Complete the form to schedule a consultation with WCG.