Carolinas Research Associates (CRA) was established in 1996 as an Investigative Site Network (ISN). In 2008 we expanded our operations to include a Dedicated Research Site capitalizing on our expertise in clinical trial management and subject recruitment. Our unique alliance with board-certified, private practice physicians gives us access to experienced investigators in a variety of therapeutic areas. We provide a single contact point for access to multiple sites with centralized contract negotiation, regulatory coordination and subject recruitment to assure efficient study start up. CRA sites offer experience, quality and longevity for your research projects.
Carolinas Research Associates has over 14 years of clinical research experience providing our sponsors with expertise in all aspects of clinical research services. We provide a management program and infrastructure which is designed to facilitate a wide spectrum of comprehensive and cost effective services. Our management staff provides administrative oversight and medical supervision for all aspects of a project from start-up to close-out. All study activities comply with ICH Guidelines and are under the scrutiny of our Medical Director. Staff members are trained to provide thorough screening and consenting of all patients to insure candidates that are well qualified for each study. Our work ethic is based on the promise that we will do whatever it takes to get the job done, and get it done right.
Our approach to clinical research is centered on the following key standards:
- Experienced Management Staff
- Professional, Dedicated, Certified CRCs
- Accurate IRB Submission and Approval
- On-site Training for Physicians and Staff
- Audit Ready Studies
- Accurate CRF Completion
- Complete Regulatory Compliance
- Professionally Developed Corporate SOPs
- Internal CAPA Program
- Effective Study Volunteer Recruitment
- Thorough Screening and Consenting of Patients
- Rapid, Responsive Communications
- Study Specific, Site-Based Recruitment Plan & Materials
- Dedicated Regulatory Specialist
Carolinas Research Associates sites are strategically located in the Piedmont area of North Carolina. The Charlotte metropolitan area spans North and South Carolina, offering access to a large and diverse population. All CRA sites are located with easy access to the Charlotte-Douglas International airport.
Placing a clinical trial with Carolinas Research Associates allows your project to proceed in a manner that will earn your confidence and maximize success for your clinical trials. CRA understands the importance of effective and timely subject recruitment for a successful trial. We have a dedicated Subject Recruitment Specialist, to develop study-specific recruitment plans to assure enrollment goals are met or exceeded for all projects. We provide access to a diverse population of study volunteers through our extensive research database and physician patient base and web based community.
