Highly qualified public health professional with extensive expertise in clinical trial coordination, protocols, and participant relationships. Proficient in medical practice and clinical research environments. Strong working knowledge of ICH-GCP, phlebotomy, biomedical and regulatory guidelines, and monitoring guides. Demonstrates effective communication skills when interacting with study participants, principal investigators, and colleagues. Experienced in oncology, bone marrow transplants, neurology, cardiovascular, sleep, communicable and chronic diseases, and nutrition. Known for initiative, organization, time management, problem-solving skills, and strong leadership abilities.
Serves as a key liaison between patients, healthcare providers, and clinical trial investigators. Guides patients through the clinical trial process, ensuring they understand the study requirements, and facilitating their participation in trials that may be beneficial for their condition.