Our Team

At NEOREX CRO, our greatest strength is our people. Our team is composed of highly experienced professionals with backgrounds in clinical operations, regulatory affairs, licensing, medical science, project management, and quality assurance. With decades of combined expertise in the pharmaceutical and medical device industries, we bring operational precision and scientific integrity to every project we manage.
Whether managing complex multi-site trials or guiding regulatory submissions across regions, our team works with focus, efficiency, and purpose.

Cross-Functional Expertise

Our integrated team brings hands-on experience in:
•  Clinical Trial Management (Phase I–IV)
•  Regulatory Strategy and Submissions
•  Licensing and Product Registration
•  Site Relationship Management
•  Feasibility and Start-Up Activities
•  Medical Monitoring and Pharmacovigilance
•  Protocol Development and Investigator Training
•  Quality Assurance and Compliance Oversight
Our collaborative, cross-functional approach ensures seamless coordination and consistent excellence across every aspect of your clinical development journey.

Scientific Leadership

Our Scientific Board is actively involved in the planning and execution of clinical studies, providing strategic and clinical input across the full project lifecycle. With top-tier specialists in oncology, internal medicine, infectious diseases, cardiology, and hematology, they help ensure every protocol is both scientifically rigorous and aligned with evolving clinical standards.

A True Partner to Sponsors

Whether you are advancing a first product or managing a global portfolio, our approach is personalized, agile, and outcome-oriented. We adapt to your needs with flexibility, transparency, and full accountability — offering customized solutions that integrate seamlessly with your organization and goals.

Company Structure

NEOREX CRO is structured to ensure both scientific oversight and operational excellence. Our organizational framework includes:
•  General Management – Strategic leadership, governance, and partnerships
•  Scientific Board – Oversight of clinical design, safety, and medical integrity
•  Clinical Operations – Project management, site management, and monitoring
•  Regulatory & Licensing Affairs – Submissions, approvals, and post-marketing support
•  Quality Assurance – Compliance, audits, and continuous improvement
•  Business Development – Client engagement and service coordination
This structure allows us to remain responsive, accountable, and quality-focused at every stage of our work.