Clinical Trial Management

Comprehensive oversight of clinical studies ensuring efficiency, compliance, and high-quality outcomes.

Study Design & Protocol Development
Design scientifically sound clinical trial protocols based on study objectives
Develop statistical analysis plan and define study endpoints
Site Selection & Feasibility
Assess clinical research center resources
Evaluate investigator capabilities and patient recruitment potential
Project Management
Comprehensive trial progress management
Risk control and quality assurance
Trial Monitoring
Regular CRA (Clinical Research Associate) monitoring visits
Ensure compliance with GCP (Good Clinical Practice)