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Federal Support > Government & Military Research

Government & Military Research

ClinicalRM works collaboratively with its Government customers to provide clinical research services from technical and clinical professionals that understand the uncertain nature of research, and how each solution will ultimately benefit the warfighter and many others around the globe.  The type of services that we provide include: 

  • Project Oversight
  • Program Management
  • Administrative Support
  • Facility and Equipment Maintenance Services
  • Pre-Clinical (GLP) Project Solutions
  • Clinical Trials Center Services
  • Biologic Manufacturing (GMP) Capabilities
  • Regulatory Oversight
  • Medical Writing
  • Data Management
  • Site Monitoring
  • GCP, GLP, GMP Training

Highly-Skilled Medical Personnel Include:
  • MD and PhD level investigators and researchers
  • Technical and Scientific Research professionals
  • Laboratory technicians

Technical and Laboratory Specialists Include:
  • System Administrators
  • System Validation Engineers
  • Electronic Document Management Specialists
  • Laboratory Information Management Systems Specialists
  • Knowledge Managers
  • SAS Programmers
  • Data Managers
  • Clinical Data Managers
  • Biostatisticians
  • Genomics Laboratory Scientists
  • Bio-analytical Laboratory Scientists
  • Laboratory Research Technicians
  • Natural Products Technicians
  • Laboratory Investigators

Comprehensive Project Services
  • Program and Project Management
  • Site Selection and Partnering 
  • Protocol Development
  • Regulatory Oversight
  • Quality Assurance and Training
  • Data Management
  • Monitoring
  • Statistical Analysis
  • Final Report Creation / Medical Writing
  • FDA Submission

Defense Acquisition Certified
ClinicalRM’s Defense Acquisition Certified staff offers clinical and regulatory data management services utilizing best-of-breed technology solutions to meet the FDA requirement for a validated system.  Our understanding of working in a federally secure environment allows for an efficient implementation of necessary processes and controls to protect the accuracy, security, and integrity of research and development products slated for regulatory approval.
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