Our Multi-Site Model
By combining our robust CRO support services and a network of over 50 strategic site partners across North America, Dr. Vince Clinical Research (DVCR) can now manage multi-site Phase I-III studies in patients, specialty populations and healthy normal volunteers across a diverse range of therapeutic areas and trial designs.
The DVCR team has significant experience managing external site activities for the seamless delivery of high-quality data to our sponsors, including external site feasibility and management. We maintain a network of strategic sites that have a diverse range of capabilities and patient populations to conduct multi-site clinical studies (Phase I-III). Our robust site feasibility and selection process ensures that the most capable sites are participating in your study and that they align with DVCR’s commitment to speed, customer service and delivering the cleanest data possible.
Our model prioritizes sites that leverage these principles to help our sponsors reach their milestones faster.
Site ID and Selection
Quality over quantity is imperative for a successful model as we are not trying to be all things to everyone.
Prioritizing Site Payments
Sites need quicker payments to avoid study delays. This reinforces our collaborative, true partnership approach.
Site Engagement
We are committed to being a true partner, providing sites with essential tools, support, and prioritizing transparent communication and collaboration.
Lead Site ModelTM
DVCR as Lead Site expedites recruitment, mitigates issues, standardizes conduct and data, and provides hands-on training for sites.
Contact us to learn more about conducting a multi-site clinical trial
