Our feasibility analysis team, comprised of Clinical Operations Directors, Recruitment Manager and Principal Investigators, provides immediate operational, safety and recruitment feedback within 24hours direct to our clients. Vince and Associates consistently provides solutions to challenging protocols, ensuring the study is successfully recruited, logistically efficient and results in the timely, superior data quality our clients require to make informed drug development decisions.


Vince and Associates Clinical Research houses a full-time recruitment and marketing team to ensure qualified, on-time recruitment using direct database outreach, as well as radio, print, television and Internet advertising to our ethnically diverse, compliant subjects in the Kansas City metropolitan area of >2 million residents.

Our state-of-the-art recruitment department provides a real-time database of >32,000 volunteers pinpoints information including demographics, specific diagnoses, concomitant medications, medical history and other characteristics. Our advanced data technologies aid enrollment by identifying populations meeting protocol criteria and allows for rapid, direct outreach.


Vince and Associates Clinical Research specializes in rapid study start-up. Regulatory documents and budgets are reviewed and submitted on average between 24-48 hours. Furthermore, our ability to utilize various central Institutional Review Boards (IRB) assures rapid protocol approval. We are consistently recognized as one of the fastest enrolling sites repeatedly for our clients.


Vince and Associates’ Quality Assurance (QA) program ensures that clinical trials are conducted per protocol and compliant with ICH/GCP Guidelines:

• Quality Assurance services led by former big pharma clinical monitors
• Comprehensive SOPs with appropriate training records
• Regulatory Affairs Advisor with >37 years of experience with the US Food and Drug Administration
• Strong foundation in ICH/GCP/CFR highlighted by completion of >60 sponsors and agency audits