Ruhana Shaikh

As a Senior Clinical Research Coordinator, I oversee the comprehensive management of clinical trials, ensuring strict adherence to protocols, regulations, and SOPs. My responsibilities span study start-up activities—including protocol review and site initiation visits—to participant recruitment and informed consent processes. I manage participant scheduling and study visits while collecting, reviewing, and accurately entering critical study data. Coordinating study procedures and managing supplies and investigational products, I maintain compliance with GCP guidelines and institutional policies, ensuring high-quality and ethical clinical research execution.