Clinical Research Professional with over 8 years of experience in managing Phase I–IV trials, ensuring compliance with GCP, ICH, and regulatory standards. Skilled in study start-up, patient recruitment, site monitoring, and data management. Proven ability in collaborating with cross-functional teams, CROs, and sponsors to produce high-quality data. Focused on advancing ethical research practices while prioritizing patient safety and protocol compliance.
Breast Oncology
Cardiology
Client Operations
Operations Department
English Department
Brain Injury Rehabilitation
Leukemia
Hard Skills
Technical Skills
Soft Skills