Skip links

Operational Support & Site Enablement with Efficient Clinical Research Staffing Services

From vacant spaces to inspection-ready research sites — Minerva provides optimal clinical research staffing, compliant infrastructure, and operational support to drive trial success.

— Quality Clinical Trial Operations & Services

Empowering Sites to Meet Global Clinical Standards

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.

Clinical Research Staffing Services

    Delivering Quality & Innovative Solutions

    Offering Foundational Support to Make Research Sites Trial-Ready

    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.

    Clinical Trial Consultant
    What we achieved

    From Infrastructure and Compliance to Operational Efficiency – We Integrate It All

    Infrastructure and Systems

    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.

    Regulatory and Compliance Support

    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.

    — Quality Clinical Trial Operations & Services

    Manage Studies Like a CRO with Clinical Research Staffing Services — Without Needing One

    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.

    Infrastructure and Operational Setup

    Set up compliant clinical space, validated systems, and workflows ready before first patient visit.

    Staffing and Associated Trainings by role

    Hire and train site staff by role with protocol, GCP, and soft skills focus.

    Finance/Accounting Support

    Assist with budget planning, contract setup, invoicing, and timely payment tracking for smooth operations.

    Risk Management

    Track deviations, conduct audits, and prepare sites for IRB, FDA, and sponsor inspections.

    Data Operations & Quality Assurance

    Ensuring clean, query-free data through real-time tracking, monitoring & centralized quality checks.

    Regulatory Affairs & Compliance

    Streamlined submissions and rapid approvals through deep familiarity with local ethics boards and regulatory bodies.

    img-3@2x

    FAQS

    We provide CRCs, regulatory specialists, study coordinators, recruitment staff, data entry, site managers, and administrative support as part of our clinical research staffing services.

    Yes. Our team enables fully operational sites by managing infrastructure setup, hiring, training, and SOP deployment.

    Through role-specific training, SOPs, compliance tracking, and centralized performance oversight aligned with GCP and sponsor expectations.

    Together We Can Build Sites That Deliver

    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.

    Trial-Ready Sites. Trained Teams. Trusted Clinical Trial Consulting Services.

    Get Started Today
    🍪 This website uses cookies to improve your web experience.
    Explore
    Drag