RMP provides comprehensive operational management for research clinics, including staffing, workflow optimization, regulatory compliance, and day-to-day operations to ensure efficient and compliant clinical trial conduct.
We provide comprehensive operational management for research clinics, including staffing, workflow optimization, regulatory compliance, and day-to-day operations to ensure efficient and compliant clinical trial conduct.
Our team assists clinics in preparing for clinical trials by evaluating operational readiness, developing protocols, training staff, and establishing infrastructure to meet regulatory and industry standards.
We ensure to streamline the acquisition for clinical research trials through our vast site network of sponsors and CRO trusted partners. This includes preparing regulatory submission documents, navigating IRB approvals, and ensuring regulatory compliance to facilitate smooth trial initiation with quick turnaround times.
Research Management Partners (RMP) delivers clinical research contract support tailored to the expectations of each site within our network. Our team reviews and clarifies site-specific terms, obligations, and compliance requirements, ensuring alignment with both regulatory standards and operational capacity. By doing so, RMP helps sites mitigate legal and operational risks while promoting full transparency throughout the contract and budget negotiation process.
Our team can assist in drafting, reviewing, and implementing SOPs for clinical research sites within our trusted network. We ensure that the SOPs are in line with industry standards and best practices while taking into consideration the clinical research sites’ infrastructure
We offer comprehensive patient recruitment solutions to ensure clinical trials meet enrollment goals efficiently and ethically.
RMP provides comprehensive budget development and negotiation services with pharmaceutical sponsors and CRO partners. We ensure fair coverage for all study-related costs, including procedures, staff time, overhead, pharmacy, and administrative expenses. Our evaluations incorporate inflation adjustments, screen failure rates, and contingency planning, maximizing reimbursement strategies for each site. By benchmarking against industry standards, RMP protects sites from underpayment and missed cost
Through its trusted network, Research Management Partners (RMP) delivers centralized staff services — from clinical operations and regulatory support to patient recruitment and financial management — allowing sites to focus on patient care while RMP drives compliance, efficiency, and enrollment success.
RMP delivers ongoing training for research staff on Good Clinical Practices (GCP) and International Council for Harmonization (ICH) annually.
For organizations seeking to develop new research sites or expand existing facilities, we offer strategic planning services and operational guidelines tailored to individual research site's needs.
RMP acts as a liaison between pharmaceutical companies, CROs, and clinical research sites. We facilitate site assessments, during the pre-qualification period through the duration of the trial. Ongoing communication is optimized to ensure engagement and proper oversight of our site management services.
MP implements structured quality control checklists to ensure that research staff and investigators adhere to protocol requirements at every stage. Our quality assurance programs reinforce Good Clinical Practice (GCP), ICH guidelines, ALCOA principles, and sponsor/CRO expectations, while maintaining compliance with regulatory reporting standards and internal site policies.
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