Your Full-Service CROTM
Company Brochure
We are pleased to share Dr. Vince Clinical Research’s latest brochure, providing an in-depth overview of our full-service CRO solutions.
Highlights include:
- Unique model for multi-site trials
- Luxurious Phase I unit
- Unsurpassed volunteer recruitment and retention
- Producing Smarter Faster Data® through seamless tech integration
UPCOMING WEBINAR
Acute Pain Models in Drug Development
Tuesday, January 28, 2025 | 1pm EST (10am PST)
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.
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.
UPCOMING WEBINAR
Acute Pain Models in Drug Development
Tuesday, January 28, 2025
1pm EST (10am PST)
UPCOMING WEBINAR
Acute Pain Models in Drug Development
Tuesday, January 28, 2025 | 1pm EST (10am PST)
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.
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.
Early Phase CRO Solutions
Dr. Vince Clinical Research (DVCR) is a full-service contract research organization (CRO) specializing in early phase trials in both healthy normal volunteers and patient populations across a wide range of trial designs and multiple therapeutic areas such as neuroscience, psychiatry, substance abuse, pain, cardiometabolic disorders, infectious diseases and others. CRO services include project management, data management, biostatistics, monitoring, PK/PD analysis, medical writing as well as site feasibility and management for multi-site trials. Additionally, DVCR operates one of the most innovative and technologically advanced clinical pharmacology units in the world with over 90 beds for overnight confinement, a cGMP compliant pharmacy as well as luxurious amenities to support diverse study participant recruitment and retention. By leveraging technology and one of the country’s most experienced leadership teams in early clinical development, DVCR provides Smarter Faster Data® to their biopharmaceutical clients.
“We created a world-class CRO by investing in people, technology and environmental sustainability.”
Bradley D. Vince, D.O. CEO & Chief Medical Officer
Speed and Diversity in Recruitment
SMARTER FASTER DATA®
Every single detail of the company and facility has been reimagined to provide the optimal environment for clinical study execution.