Senior Clinical Research Associate with over 8 years of experience managing and monitoring Phase I-IV clinical trials, specializing in regulatory compliance, patient safety, and data integrity. Proficient in site management, conducting site visits, and ensuring adherence to study protocols. Skilled in stakeholder collaboration, risk mitigation, and using industry-standard EDC and CTMS platforms. Adept at driving successful trial outcomes through strong communication and problem-solving. Seeking to apply extensive clinical research expertise in a new, challenging role focused on advancing high-quality research and therapeutic development