Clinical Research Consulting & Education Services, LLC

Building & Enhancing Compliance

Education is Key

Clinical research organizations realize that the burden of maintaining an in-house team of clinical research experts is expensive and isn't sustainable. Some organizations lack staff who fully understand regulatory operations and financial aspects of regulations associated with clinical research. Maintaining a compliant clinical research program is accomplished by continuously educating staff who support the clinical research portfolios.

CRCES offers educational curriculums for faculty, regulatory staff, and finance teams. We will work with your organization to develop a curriculum that meets your organization's needs. CRCES' consultants can provide synchronous and asynchronous training opportunities.

Struggling with Managing Your Clinical Research Program?

Managing quality, risk and compliance has never been more important for organizations involved in clinical research. Most organizations find it quite challenging and expensive to assemble and maintain an experienced clinical research operations team. Fragmented business processes and technology that hasn't been optimized for managing clinical research operations hinder compliance goals.

CRCES' consultants can help. Our content experts are pharmacists, laboratory specialists, and financial specialists with proven track records in their area of expertise.

Teamwork to Accomplish Organizational Goals

Clinical Research Consulting & Education Services, LLC (CRCES) provides clinical research consulting, auditing, and education services for life science, pharmaceutical, clinical research organizations, and health systems.

Creating Best in Class Standards

Standardize guidelines, processes, metrics, targets and plans across the organization;
Lead, align and cascade operational excellence; and
Effectively integrate operational excellence into daily operations for more efficient and consistent performance.

CRCES provides:

Develop/enhance clinical research program to include human subjects protection, research pharmacy
Develop/enhance clinical research billing program
Support drug approvals and FDA regulations
Clinical research billing audit
Optimization of clinical research technology solutions to include CTMS and EHR
Development of key metrics and performance indicators
Education services for clinical research personnel