Site Collaboration | Patient-Centered Delivery
Our Focus
LunaClinical delivers hands-on support at trial sites, comprehensive regulatory coordination, and sponsor-level execution—led by our award-winning clinical researcher and backed by nationally experienced CRAs, based in the U.S. and supporting sites worldwide.
Therapeutic areas include immunology, neurology, oncology-device, CNS (including depression/MDD), ophthalmology, and infectious diseases.
What We Offer:
1. Clinical Research Consultant (On-site / Remote)
Independent CRA support across diverse therapeutic areas, providing flexible, sponsor-aligned oversight.
2. Site Monitoring & Visit Reporting
Comprehensive pre-study, initiation, interim, and close-out visits with clear, timely monitoring reports.
3. Study Start-Up Coordination
Support for feasibility, site selection, regulatory submissions, and readiness tracking.
4. Protocol Compliance Oversight
Ongoing evaluation of site performance, deviation tracking, and issue resolution to ensure protocol adherence.
5. Data Review & Query Management
EDC review and timely resolution of data queries to maintain data quality and integrity.
6. Patient Recruitment & Retention Support
Collaboration with sites to implement strategies that improve enrollment and minimize dropout.
7. Regulatory Document Support
AssIstance wIth site regulatory binder setup, ICF review, and essential document tracking and submissions.
8. Cross-Functional Collaboration
Coordination with study teams, vendors, and site staff to ensure efficient communication and trial execution.