SPONSORS Proven performance
WHY CHOOSE PRECISION?
We are not your typical research site.
Since 1999, Precision Clinical Research has conducted hundreds of clinical trials with great success
by continually delivering on our promises of unparalleled service and exceptional performance.
All our investigators are leading private practitioners in the South Florida area with years of research experience, and the majority of our research staff has worked here for over a decade. Over 90% of our study participants come from our private practice database, most of them with complete medical records. Our experience in the clinical research makes us the preferred choice of Sponsors and CROs in a wide range of indications.
Precision Clinical Research was selected as a finalist for the Society for Clinical Research Sites’ Site Patient Recruitment Innovation Award (SPRIA) at the 2015 Site Solutions Summit.
We believe great research starts with the patient, and we strive to provide our patients with the best medical team available.
Our investigators are the top investigators within the community with years of research experience with access to several hundred thousand patients and their electronic medical records. We are not the typical site that relies on advertising or other methods to meet enrollment goals. We primarily recruit study subjects from our established practice database. This allows our site to prescreen potential study subjects prior to scheduling a screening visit in an effort to keep screen failures to a minimum.
We have a research team second to none.
We employ research coordinators and administrative support personnel. Our research coordinators are typically RN’s, LPN’s, Med Tech’s and have extensive experience in the research field often with specialty certifications within the clinical research industry. Our administrative team consists of patient recruiters, regulatory administrative personnel, coordinator assistants, dedicated EDC entry personnel, and experienced business administrators. From Site Selection through Study Close Out, you will find that our patient-centric organization ensures consistency, compliance, and the highest quality performance and results.
Feasibility questionnaires are completed quickly and answered honestly WITH a bias towards being conservative. Our turnaround time to submit regulatory documents and review contractual agreements is usually less than 7 days.
We are one of the top selected research sites by major pharmaceutical companies based on our past performance by meeting enrollment goals and the quality of our timely data. We have been in clinical trials since 1999, and we have the recruitment metrics to back up our claims:
studies since opening in 1999
patients for a study in just 1 month
We conduct trials across
of our enrollment goals