Integrated sites.
World-class recruitment.
Your dedicated research partner.
Whether you’re ready to conduct a single-site study or a complex, high-volume clinical trial, trust Velocity to deliver the the right investigators, clinical staff, and patients.
80
Clinical research sites across the U.S. and Europe
220
Investigators across multiple therapeutic areas
15,000+
Clinical trials conducted since 1986
100,000+
Participants enrolled in studies worldwide
Velocity was built to ensure sites work the way you’ve always wanted — with unprecedented quality, efficiency, and predictability.
The investigative research site organization built for the new era of clinical research
Velocity is structured to ensure sites work the way you’ve always wanted — with unprecedented quality, efficiency, and predictability.
Velocity is led by experts with extensive CRO experince. Together, we've investigative research site organization built for the new era of clinical research.
Site ID
Integrated site operations
Fast and effortless site identification and contracting processes for you
Streamlined start-up processes
Centralized study initiation activities and digitized source, regulatory, and records management
World-class patient engagement
Dedicated teams drive industry-leading enrollment and retention programs
In-house quality and data management
Intensive monitoring and quality oversight programs supported by a unified technology system to ensure accurate data delivery
Fully integrated operations to support rapid site identification
Above all, Velocity is structured to increase the quality and efficiency of clinical trials. This starts with you. Before trials even begin, Velocity is committed to simplifying your site identification processes and enrollment forecasting. And your trial management team can expect the same advantages downstream — centralized communication, consistent site processes, and industry-leading oversight.
Many of Velocity's investigators are even sought after to assist with protocol design, providing insight to reinforce the viability of research programs. Their expertise, paired with Velocity's centralized model, facilitates more efficient and predictable trial performance.
- 48-hour turnaround on contract/budget responses
- One contract for all Velocity sites in your study
- One point of contact ensures seamless communication
- Simplified site assessment across 80 sites, 220 investigators
- Tech-enabled enrollment forecasting based on your protocol, not the indication
Standardized processes to drive streamlined start-up
With digitized source, regulatory, and records management, Velocity can quickly initiate trials and scale your trials as needed.
Beyond accommodating the soft infrastructure required to support your study, Velocity can also integrate new or unique technologies or treatment approaches to run specialized studies, decentralized trials, or hybrid studies.
- 30 days from study award to site initiation visit
- PBMC processing capabilities and on-site labs for some sites
- Integrated tech for payment/stipends, eReg, EMR/HER, same-day collection/shipping
- Study start-up training meetings with site staff
- Clinical data specialist assigned to every study
- Alignment with your central IRB or central laboratory
World-class patient engagement and retention solutions
Velocity is built to accurately forecast and meet enrollment and retention targets, particularly for high-volume and hard-to-recruit research programs. With four fully-owned Patient Engagement and Recruitment Centers, Velocity is constaly improving recruitment, screening, consenting, retention, and follow-up processes for clients and participants alike.
Every Velocity site is also supported by full-time recruitment specialists to drive local outreach. Sites are located in demographically diverse areas to support proportionate representation in clinical trials.
- Immediate enrollment support upon study start
- Access to proprietary, physician, and practice databases
- Intensive community outreach and diversity initiatives
- In-house advertising solutions that outperform central campaigns
- Participant adherence and retention programs
- Specialty care sites provide access to niche populations, procedures, and facilities
Uncompromising quality and accurate data delivery
Velocity has created a unique, industry-leading quality oversight model. All Velocity sites and studies are supported by in-house clinical data, quality assurance, regulatory, and risk management teams.
These veteran teams work directly with site staff, serving as a resource to help identify — and leverage — areas for continuous improvement. The teams support all aspects of QA/QC processes to ensure adherence to all applicable FDA regulations, ICH GCP Guidance, state guidelines, industry standards, and Velocity's own stringent SOPs.
- 48-hour data entry target; query resolution within 48 hours of query generation
- Routine and random QA reviews; EDC and source cross-checks
- Commitment to routine investigator and site staff training
- CLIA-certified labs, IATA-certified staff, GCP-trained physicians and staff
Simplify everything from site identification to study close-out.
Velocity unifies operational processes to provide world-class sites and predictably high performance for your trials.
