Site-level clinical support across the network.
Dedicated Investigators Advancing Clinical Research and Patient Care.
RMP’s sub-investigators support enrollment, safety oversight, and day-to-day protocol execution within our centralized operational framework. These practitioners bring prior clinical trial involvement through their work as referring physicians, sub-investigators, or both, combining clinical care experience with an understanding of the research process.
RMP continues to expand its roster of sub-investigators and specialty practices. Individual experience varies by practitioner; detailed investigator CVs and site-specific experience are available upon request or during feasibility discussions.
Meet Our Sub Investigators
Our network of Principal Investigators includes board-certified physicians and experienced research leaders across multiple specialties, all committed to advancing medical science through high-quality clinical trials. Each investigator is supported by RMP’s centralized operational, regulatory, and quality oversight frameworks.
Why Sponsors Choose RMP
Our dedicated research teams work closely with Sponsors and CROs to support:
- Access to Oncology Patients
- Integrated Clinical
- Workflows
- Biospecimen Collection Support
- Centralized Quality Oversight
- Multi-Site Scalability
- Experienced Investigators
Biospecimen Collection & Laboratory Partnerships
RMP collaborates with experienced laboratory partners supporting:
- Blood Collection
- Tissue Collection
- PBMC Processing
- Biomarker Analysis
- Genomic Testing
- Sample Processing & Storage
- Chain of Custody Management
- Protocol-Specific Laboratory Workflows
