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SPONSORS & CROs

What to know

American Carolina Clinical Research (ACCR) is dedicated to improving healthcare through ongoing and systematic clinical research trials. Our team of experienced principal investigators, sub-investigators, study coordinators and other site staff conducts high-quality clinical trials in collaboration with leading pharmaceutical and biotech companies. Our research covers a broad range of therapeutic areas, including but not limited to COPD, pediatrics, family practice, GI, Mental Health, Hematology-Oncology, Internal Medicine and Nephrology. As an experienced clinical trial facility, we serve children and adults throughout the Carolinas. We utilize cutting-edge scientific methods and technologies to ensure that our studies are accurate, reliable, and relevant. At ACCR, we are committed to advancing medical knowledge and improving patient outcomes through ethical and scientific clinical research. Join us in our mission to improve healthcare outcomes.

SERVICES

Experienced in clinical research services

Conducting Clinical Trials

Our expertise lies in conducting diverse clinical trials with a focus on patient safety, regulatory compliance, and scientific excellence to advance medical knowledge and bring new treatments to patients.

Patient Recruitment

Efficient and effective patient recruitment services for clinical trials, utilizing various strategies to identify and enroll eligible participants, while prioritizing patient safety, privacy, and engagement.

Clinical Research bootcamp

Clinical research bootcamps provide a comprehensive, intensive and accelerated curriculum, offering hands-on experience and practical skills to individuals seeking to begin or advance their careers in clinical research.

Community Outreach ‚Äč

Community outreach refers to the process of engaging and educating the local community about clinical research and its potential benefits. Our team provides comprehensive community outreach services to build awareness and trust, and facilitate enrollment of diverse study populations.

Contract (Clinical Trial Agreement)/Budget Development

Contract and budget development involves negotiating and creating contracts and budgets for clinical trial agreements between sponsors, CROs, and research sites. Our team provides guidance and support in developing fair and reasonable contracts and budgets that align with the needs of all parties involved, ensuring successful collaboration and conduct of clinical trials.

site staff training

Our team provides comprehensive site staff training programs covering key topics such as study protocols, patient recruitment, data management, and regulatory compliance to ensure efficient and compliant clinical trial conduct.

Regulatory (IND, IDE)

Regulatory services involve ensuring compliance with regulatory requirements for clinical research studies, including filing for and maintaining an Investigational New Drug (IND) or Investigational Device Exemption (IDE). Our team provides guidance and support throughout the regulatory process to ensure successful approval and conduct of clinical trials.

Internship Programs

Our internship programs in clinical research provide hands-on experience and practical skills to individuals seeking to enter or advance their careers in the field. Programs are tailored to meet specific industry needs and include study coordination, data management, and regulatory compliance.

Study Sponsor Request