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BHR Consulting Group is our division committed to assisting clinical research sites in efficient management through cost-effective clinical research operations services at the site level, providing a more economical alternative to maintaining an in-house research staff.

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Gone are the days when the Clinical Research Coordinator handled all tasks, leading to numerous follow-up action items and subpar clinical research conduct. Your coordinator should prioritize patient care, while we manage your administrative needs to guarantee seamless site operations.

  • Quality Assurance

Ensure precision with the expertise of our specialists in quality assurance. Tailored to your site, our QA program includes daily source reviews, monthly on-site monitoring visits conducted by our in-house Quality Assurance Specialists.


  • Source Document Creation

Creating source documents can be burdensome. Allow us to generate your sponsor-approved source documents, freeing you up to focus on other essential tasks.


  • Data Entry/Query Management

Timely EDC Data Entry is critical to the success of the drug approval process. Research Coordinators can now focus on patient care and protocol guidelines without the stress of EDC entry and Query Management.


  • Regulatory Management

From study initiation to closure, BHR Consulting Group provides a dedicated regulatory specialist to act as the intermediary between your clinical site and sponsor. With a 48-hour turnaround for all regulatory requests, ISF and eISF management, and IRB submissions, our dedicated regulatory specialist will support all your regulatory needs.

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