DJL Clinical Research
DJL Research is a full-service clinical research partner based in Charlotte, North Carolina. It operates as an Investigative Site Network dedicated to optimizing and streamlining clinical research operations for physicians within their practice. Founded by Dr. Jane Box and Dr. Patrick Box, the company focuses on enriching patients' lives through innovative therapies, assisting physicians in developing high-quality research departments, providing sponsors with efficient trial management, and fostering a collaborative environment for growth and learning. With over 25 years of experience, DJL Research offers extensive physician training, manages trial processes, and connects practices to a broad spectrum of clinical indications and sponsors.
Industries
Nr. of Employees
small (1-50)
Services
Act as a single administrative contact handling communications and coordination between sponsors/CROs and network sites.
Partner with independent physician practices to integrate clinical research into daily practice with minimal upfront costs.
Oversee regulatory documents, coordinate IRB approvals, and manage informed consent procedures for studies.
Prepare and manage study budgets and contracts for participating network sites and physician practices.
Provide onsite and ongoing training for investigators and coordinators plus a consistent QA program to improve processes across the network.
Use a multi-specialty network database to support recruitment across a range of indications and improve enrollment rates.
Act as a single administrative contact handling communications and coordination between sponsors/CROs and network sites.
Partner with independent physician practices to integrate clinical research into daily practice with minimal upfront costs.
Oversee regulatory documents, coordinate IRB approvals, and manage informed consent procedures for studies.
Prepare and manage study budgets and contracts for participating network sites and physician practices.
Provide onsite and ongoing training for investigators and coordinators plus a consistent QA program to improve processes across the network.
Use a multi-specialty network database to support recruitment across a range of indications and improve enrollment rates.
Expertise Areas
- Clinical trial management
- Investigative site network operations
- Patient recruitment and enrollment
- Regulatory compliance and IRB coordination
Key Technologies
- Centralized administrative site network model
- Clinical data management systems
- IRB and informed consent workflows
- Site monitoring and audit readiness processes