Experienced Clinical Trials Coordinator with over 21 years in clinical research and 17 years in administrative support, specializing in endocrinology, infectious disease, nephrology, and oncology. Proven ability to manage complex clinical trials from initiation to close-out, ensuring regulatory compliance and high-quality data collection. Skilled in strategic planning, stakeholder coordination, and project management, with a strong focus on process improvement and operational efficiency. Adept at navigating IRB submissions, conducting compliance audits, and supporting change management initiatives. Demonstrates exceptional analytical skills, attention to detail, and commitment to participant safety and ethical research practices. Proficient in a wide range of clinical trial platforms and systems, with a reputation for outstanding customer service and cross-functional collaboration.