Site Capabilities
Our pharmaceutical and CRO partners are so important to us and we accomplish a lot together. We understand what it means to bring a clinical trial from site activation to study closeout while providing clean and timely data in between. The majority of our patients come from our physicians' private practice databases.
Principal Investigator Oversight & Data Integrity
A clinical trial is only as safe and successful as is the involvement of the Principal Investigator. With dedicated full-time investigators with their own built-in private practices onsite, The Probe brings a highly sought after offering of research-naive patients, and strong safety oversight to the studies it undertakes.
Operating With Site Metrics In Mind
In the age of Risk Based Monitoring and Site Metrics, The Probe formats its internal processes around ever-changing Sponsor requirements. We understand the importance of clean and reliable data, and our staff are trained on responding to data issues rapidly and effectively. With dedicated data specialists onsite, our streamlined approach allows us to provide timely and accurate results to sponsors.
Executive Team & Expertise
Our executive team understands research. The Probe can assure sponsors and CRO's that our leadership values the same KPI's that they do. The study coordinator is the backbone of any clinical research project. Not only are our coordinators amongst the most experienced in the industry, but they understand the importance of screening and enrolling appropriate study participants. The Probe prides itself on being amongst the top sites when it comes to the "initiation to first patient in" metric according to multiple sponsors and CRO's.
We are experienced in the following indications across Phase1-4 inpatient and outpatient trials:
General Medicine
Obesity
Diabetes
Hypercholesterolemia
Asthma
Alzheimer’s Disease
Ulcerative Colitis
Irritable Bowel Syndrome
Crohn’s Disease