LunaClinical provides on-site and remote CRA and study support, from start-up through close-out, with sponsor-aligned oversight and inspection-ready documentation.
in clinical research
About LunaClinical
LunaClinical is a founder-led clinical research consultancy, established in 2025 by Samuel D. Okafor, PharmD, a Clinical Research Associate with experience across Phase I–III trials in immunology, neurology, CNS, oncology‑device and ophthalmology.
We support research sites through on-site and remote monitoring, with a focus on informed consent, eligibility, safety reporting, CAPA resolution, and inspection readiness. Our work is grounded in clinical expertise and the realities of site operations.
Founder’s Credentials & Recognition
- 2024 PharmaTimes Clinical Researcher of the YearThe Americas, Gold (Global Project Team category)
- Harvard Medical SchoolPostgraduate Certificate ProgramsFoundations of Clinical Research (FCR)
Global Clinical Scholars Research Training (GCSRT) - Doctor of Pharmacy (PharmD)University of Debrecen, Hungary
Services
Flexible support across the study lifecycle, tailored to sponsor and CRO needs.
LunaClinical works alongside research sites, sponsors and CROs to keep studies compliant and data reliable. Engagements can be short‑term or ongoing, scaled to each study.
Study Start-Up
Feasibility, site selection, regulatory submissions and site readiness.
Site Monitoring
PSV, SIV, IMV and COV visits, on-site or remote, with timely reports.
Clinical Research Consultant
Flexible on-site or remote support across therapeutic areas.
Protocol Compliance
Oversight of protocol adherence, deviations and CAPAs.
SDV, SDR & Queries
Source data verification, review and EDC query resolution.
Risk-Based Monitoring
Centralized oversight using data trends and proactive site engagement.
TMF & Audit Readiness
TMF/ISF review for complete, inspection-ready documentation.
Regulatory Documents
Binder setup, ICF coordination and submission management.
Recruitment & Retention
Site strategies to drive enrollment and reduce dropout.
Cross-Functional Collaboration
Aligning sponsors, vendors and sites for timely execution.
Therapeutic experience
Hands-on trial experience across these indications and areas.
Let's work together
For CRA support, consulting enquiries or collaboration, reach out directly.