Thank you for considering Clinical Trials Research as a potential site for your current and upcoming studies. 

CTR brings the experience, the team, the facilities, the dedication and the reaction time to positively impact your study enrollment objectives. We have excellent relationships with many Sponsors and CROs as a result of our responsiveness and delivery of high quality data since 1992.

If you are tasked with identifying high performing sites for your current and upcoming studies, I would like to be given the opportunity to demonstrate how my team can become an ongoing asset to you and your company in meeting study enrollment objectives.

Please download our Site Synopsis which covers:

1.  The CTR Team
2.  Study Background (260+)
3.  Therapeutic Areas
4.  Population & Reach
5.  Facilities
6. Patient Diversity
7.  Key reasons for selecting CTR

• 300+ completed Phase 2, 3 and 4 trials since 1992;
• 100% research focused Principal Investigator since 2010;
• Large team including 3 Sub-Investigators, 4 Study Coordinators, 2-member\dedicated recruitment department and support staff;
• Adjoining medical practice for which Dr. Wayne serves as supervising Physician;
• Comprehensive Physician Principal Investigator oversight including creation of source documents for all studies, frequent daily meetings with Study Coordinators and Recruitment team as well as new study startup (feasibility questionnaire and assessment, contract/budget, regulatory);
• 19,000 patient database (CTR + Lincoln Family Practice);
• Highly refined recruitment processes and dedicated resources;
• Broad therapeutic area coverage;
• Able to accommodate studies requiring blind and unblinded staff;
• Ability to perform medication infusion and injection studies, extended site visits such as serial lab draw and serial spirometry;
• CLIA certified labs (both sites);
• Labs (local and central);
• Secure and temperature controlled drug rooms;
• Imaging (comprehensive);
• IRB approved Pre-Screening ICFs (Spirometry, HbA1c, BP, Lipid, ALT, PSA, eGFR and UACR);
• Extensive hands-on experience with major IRT/EDC systems (ClinTrak, Fusion Axiom, IBM, Inform, Medidata Rave, Oracle);
• Specialty Services (Sub-Investigators and Consultants);
• Established and active SOPs (regularly updated);
• Current GCP and IATA certifications.;
• In good standing with ACRP;
• FDA Regulated Business.