Launching a clinical trial site takes more than just space and ambition. Minerva Research Solutions builds fully operational, GCP-compliant clinical trial sites, complete with clinical research staffing solutions, SOP-aligned systems, and inspection-ready infrastructure. Our goal is to propel sites from the ground up, ensuring quality, speed, and scalability from day one.
Delivering Quality & Innovative Solutions Minerva hires and trains site personnel by role, from CRCs and regulatory coordinators to data entry and front-desk staff. Every team member is protocol-ready, GCP-trained, and equipped with soft skills for patient interaction. Our training framework ensures readiness from day one, reducing ramp-up time, and increasing protocol adherence. Furthermore, we offer feasibility assessments and protocol alignments, as well as clinical trial startup services prepared by our team (not outsourced). In addition, our project managers track milestones, compliance, and communication while maintaining coordinated contact with CROs and Sponsors. From compliant clinical spaces, IP storage areas, and lab setups to validated IT systems, Minerva ensures every site is physically and operationally ready before the first patient visits. Our regulatory and compliance team tailors SOPs to each site while aligning with international standards like ICH-GCP and managing a complete IRB/EC submission lifecycle. Our approach requires minimal oversight. Sponsors and CROs can focus on strategy while Minerva handles site readiness, clinical research staffing services, training, and operations, fully aligned with ICH-GCP and regulatory expectations. With Minerva, you get efficiency, quality, and accountability — not more handholding. Set up compliant clinical space, validated systems, and workflows ready before first patient visit. Hire and train site staff by role with protocol, GCP, and soft skills focus. Assist with budget planning, contract setup, invoicing, and timely payment tracking for smooth operations. Track deviations, conduct audits, and prepare sites for IRB, FDA, and sponsor inspections. Ensuring clean, query-free data through real-time tracking, monitoring & centralized quality checks. Streamlined submissions and rapid approvals through deep familiarity with local ethics boards and regulatory bodies. Whether you’re a sponsor launching a new study or a research site looking to expand capacity, Our team also supports staffing for clinical trials, clinical research startup support, and serves as your clinical trial consultant when needed. With expertise in cro and consultant clinical trial solutions, we also offer targeted clinical trial consulting services for scalable and strategic growth. — Quality Clinical Trial Operations & Services
Empowering Sites to Meet Global Clinical Standards
Offering Foundational Support to Make Research Sites Trial-Ready
What we achieved
From Infrastructure and Compliance to Operational Efficiency – We Integrate It All
Infrastructure and Systems
Regulatory and Compliance Support
— Quality Clinical Trial Operations & Services
Manage Studies Like a CRO with Clinical Research Staffing Services — Without Needing One
Infrastructure and Operational Setup
Staffing and Associated Trainings by role
Finance/Accounting Support
Risk Management
Data Operations & Quality Assurance
Regulatory Affairs & Compliance
FAQS
Together We Can Build Sites That Deliver
Trial-Ready Sites. Trained Teams. Trusted Clinical Trial Consulting Services.