
Clinical research professional with robust background in clinical trials and patient care. Demonstrates strong analytical skills, proficiency in medical research protocols, and ability to adapt to evolving clinical environments. Skilled in patient assessment, ethical research practices, and maintaining regulatory compliance.
I managed and coordinate clinical trial activities from initiation through patient follow-up. I review study protocols, screen and enroll eligible patients, order and track required laboratory tests and procedures, and ensure accurate documentation. I educate patients and families about investigational treatments, obtain informed consent, and maintain clear communication with sponsors and the principal investigator. I was responsible for safety and adverse event reporting, data collection and entry, participation in monitoring and audits, and mentoring research staff to maintain regulatory compliance and high-quality research standards.