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
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.