• Versatile clinical research professional with 1.6 years of experience in the pharma/life-science companies.
• Communicate with RSC and sponsors to ensure proper site management.
• Skilled in coordinating patient information,data collection, and compliance documents for diverse clinical trials.
• Highly organized with strong planning and problem-solving abilities, ensuring efficient scheduling, coordination, and documentation.
• Experienced in clinical operations, clinical data management, project management, clinical trails.