
Detail-oriented and compassionate healthcare professional with over 13 years of experience in patient care, clinical research, and healthcare operations. Proven ability to coordinate complex clinical studies, ensure regulatory compliance, and provide exceptional patient support in fast-paced hospital settings. Skilled at collaborating with multidisciplinary teams while maintaining high standards of patient care, organization, and confidentiality.
Coordinated research protocols, ensured study compliance, and facilitated clinical trial participation for Radiation/Oncology department. Maintained accurate and confidential research records, databases, and study documentation. Scheduled participant visits and facilitated communication among physicians, research staff, and patients to enhance study workflow. Tracked study timelines, adverse events, and protocol deviations to ensure quality and compliance. Assisted investigators with data collection, reporting requirements, and audit preparation. Provided compassionate support and education. to patients participating in clinical trials.
Assisted with patient preparation, mobility, transfers, and comfort to support smooth care and recovery. Provided non-medicated care such as dressing changes, skin protection, and use of supportive devices. Managed supplies, equipment, and logs to support infection.