CRP is a dedicated Clinical Research site at the forefront of clinical research, partnering with industry leaders to improve patient outcomes.
Our staff is diverse, just like the community and study participants we serve. We foster a culture that embraces diversity in all forms.
Our fully electronic Clinical Trial system allows us to minimize administrative burden and streamline operations so our team can focus more on patient engagement and protocol adherence.
Our participants are the reason we come to work every day. Our decisions and daily processes are guided by the principle that participants will always be the heart of our work.
We are proud of our committed research team, most of whom have been with our site for over 15 years. Our cohesiveness as a team and our collective experiences enable us to develop innovative solutions for the complex needs of our clinical trials.
A fully electronic Clinical Trial Management System, with remote monitoring capabilities, allows us time to focus on participants.
Our state-of-the-art research facility has three exam rooms and dedicated coordinator offices for the comfort of our participants
All studies conducted under FDA oversight with Investigational New Drug authorization.
Every protocol reviewed and approved by an independent Institutional Review Board before enrollment begins.
Patient data protected under strict HIPAA privacy and security standards at every stage of the research process.