Center for Clinical Research
Researching for Today,
Providing Answers for Tomorrow.
Serving North Carolina and the East Coast.
See If You Qualify To Participate
Disclaimer: This form is intended for general inquiries only. Please do not submit personal health information, medical questions, or sensitive data through this form.
Getting Started has never been Easier
Here at CCR we are eager to discuss more about your specific pain.
Get StartedStep 1
Contact our Recruitment Specialist
Register on this portal, by phone call or by email.
- Heather Reyna: 336-765-6181 ex 153
- recruitment@ccrpain.com
Step 2
We Will Coordinate Collection of Your Pain History
- We will review your medical history, and collect a medical release form
- We discuss open study opportunities, send you study overview information with your specific interest
Step 3
We Will Schedule Your Screen Visit
- We coordinate best time for you to come in for a Screen Visit Appointment with our Research Team
- We typically schedule your visit within 24hrs from our initial contact
Leading the Future of Pharmaceutical
& Medical Device Research
Our Medical Doctors are Key Opinion Leaders in the Research Industry with 30+ years Clinical Research Experience.
Experience and Practicality
- Single point-of-contact for fast budget and CTA agreement.
- Regulatory Specialist for quick Central Submission – Central IRBs
- 30+ years of experience in clinical research arena
- Successful plan for enrollment from diverse communities
- Decentralized trial capabilities and experience
- Principal Investigators Key Opinion Leader in Chronic, Acute, and Neurologic Pain.
- Experienced team of clinical research coordinators- average tenure 12+ years
- In-house recruitment team for rapid subject enrollment- setting multiple recruitment strategies
Participate In Research Studies
People like you make the difference! By participating in a research trial, you can play a part in helping physicians and other researchers develop and test better ways to diagnose and treat people with chronic pain. As a research participant, one learns more about the causes of specific chronic pain and how to better manage these conditions.
Therapeutic Areas
We have experience conducting clinical trials across therapeutic area of: acute, chronic, and comprehensive pain. Other therapeutic areas, including family practice, internal medicine, neuropathic pain, and others.
Regulatory Management:
We have a deep understanding of local and global regulations, and we work with you to navigate the complex regulatory landscape. Our team provides guidance on regulatory submissions, compliance requirements, and audit/inspection preparation.
Study Types
We manage a range of study types, including Phase I-IV trials, post-marketing studies, and real-world evidence studies. Our team has experience managing all types of clinical trials, and we work with you to ensure that your study meets its objectives.
You can make a difference! Please consider becoming a research participant today.
Check Out Our FAQ's
Have questions about our services? We’re here to help! Contact us anytime, and our expert team will provide the answers and support you need.
What is a clinical research study?
A clinical research study is a carefully designed investigation that helps researchers evaluate new medications, medical devices, or treatment approaches. Every study follows strict safety guidelines and is conducted according to approved protocols to advance medical knowledge and improve patient care.
Who can participate in a clinical trial?
Each study has its own eligibility criteria based on factors such as age, medical history, current health, and specific conditions. Some studies are designed for individuals with certain health conditions, while others seek healthy volunteers. Our research team will review your information to determine whether you may qualify.
Is participation safe?
Participant safety is our highest priority. All clinical studies are reviewed by an Institutional Review Board (IRB) and monitored to ensure ethical and scientific standards are met. Before joining a study, you'll receive detailed information about the purpose, procedures, potential risks, and possible benefits so you can make an informed decision.
Will I be compensated for participating?
Many clinical research studies provide compensation for your time and travel. Compensation varies by study, and our team will explain any available compensation during the screening process.
How do I get started?
Getting started is easy. Simply contact our research team or complete our online form. We'll discuss your health history, answer your questions, and help determine whether there's a study that's a good fit for you. Participation is always voluntary, and you may choose to withdraw from a study at any time.
The Center for Clinical
Research
CCR is a leading clinical research site that was founded in January 2000 by Dr. Richard Rauck and supported by Key Opinion Leaders in the Industry. CCR offers a range of services to help organizations conduct close-loop clinical trials for pharmaceutical and biotech development with both Investigational New Drug and Investigational Device Exemption.
The company has been successful and able to grow and thrive due to our dedicated team and core focus on high quality data collection. Our team has 20+ years’ experience conducting clinical trials in many therapeutic areas; specific to chronic/acute pain, comprehensive pain management
CCR also uses innovative techniques and technology to enhance the quality and efficiency of its work while adhering to regulatory requirements and industry standards. This includes using advanced patient reported outcomes to improve results for clinical studies.
In addition to providing services across many areas of clinical research, CCR has also developed a reputation for being very responsive when it comes to delivering results quickly – even at times when deadlines are tight!
Company Capabilities
We provide the following services as part of clinical site management:
- Contract and Budget Negotiation
- Drug/Device Accountability
- Electronic Data Capture – all EDC platforms
- Execution of Confidentiality Disclosure
Agreements - Invoicing- Advarra
CTMS - IRB Submission and
Correspondence - Marketing and Advertising
- Protocol Feasibility
- Query Resolution
- Record Archiving
- Regulatory and Startup Document Completion
- Site Initiation
- Site Selection Process
- SOP Development and Implementation
- Source Document Generation
- Study Closeout
- Study Execution
- Study Identification
- Subject Study Visits- onsite and remote
World-Renowned Physicians
Center for Clinical Research is home to some of the world’s most highly skilled and recognized practitioners in pain management. Our physicians are experts in a wide array of specialized services, and we pride ourselves on being on the forefront of new treatments.
Quick Links
-
Winston-Salem Office
145 Kimel Park Drive, Suite 330
Winston Salem, NC 27103 336-265-1101 Ext. 153