We are dedicated to delighting our sponsors, from rapid study start up and solid enrollment, to remote monitoring access and streamlined communications
CCT works with hospitals, health systems, academic medical centers and physician practices across the country to evaluate and support clinical research programs. We make it as easy as possible to work with our network of sites. With one call, you will have access to multiple healthcare organizations across the country and investigators representing nearly every therapeutic area.
INDUSTRY LEADING TURN-AROUND TIMES
CCT‘s network of healthcare organizations is efficient and focused, which produces industry-leading turn-around times on documents and processes essential to quick study start.
- CDA execution
- Feasibility questionnaire
- IRB time to notification
- Contract approval
- Budget approval
- Study activation timeline
- CRF and query reports
- 2 days
- 2 days
- 2 weeks
- 1 week
- 1 week
- 2-4 weeks
- 3 days
EXPERIENCED AND TRAINED PIs
- Dermatology
- Dental
- Internal Medicine
- Cardiology
- Ophthalmology
- Oncology/Hematology
- Orthopedics
- Otolaryngology
- Pediatrics
- Endocrinology
- Gastroenterology
- Infectious Disease
- Nephrology
- Podiatry
- Psychiatry
- Rheumatology
- Psychiatry
- Family Medicine
- OB/GYN
- Rheumatology
- General Surgery
- Bariatric
- Plastics
- Reconstructive
- Vascular
- Urology
- Wound Care
- Veterinary
HOW CCT WORKS
When a trial opportunity is brought to CCT, we meticulously evaluate the protocol to gauge:
- Investigator interest
- Patient population and enrollment potential
- Study coordinator experience and current workload
- Feasibility within the hospital and clinics
Once we determine that a trial is a good fit, we work with our sponsors every step of the way to move the trial quickly through the start-up process. We believe clinical trial success depends on solid sponsor-site communications, so we develop plans to ensure ongoing contact and feedback. Prior to study activation, we develop a comprehensive enrollment strategy and logistical plan, including investigator and staff training, to ensure compliance and to meet enrollment goals.
GET IN TOUCH
We want working with CCT to be a pleasure for pharmaceutical companies, device companies, biotech companies and CROs. Our focus on your strategic priorities and our attention to every detail of the clinical trials process ensure both a positive outcome and a positive experience for our trial sponsors.
Contact us as you look to place your next trial. You’ll experience the CCT difference.