

Detail-oriented Clinical Research Coordinator with over 2 years of experience managing Phase II–IV clinical trials across Oncology, Rheumatology, Pulmonology, and Critical Care. Expertise includes patient recruitment, informed consent, protocol implementation, regulatory documentation, and data management. Collaborates effectively with investigators, sponsors, and CROs to ensure compliance with ICH-GCP standards and maintain participant safety.
ICH-GCP
Quality assurance
Data management
Project Coordination
Stakeholder Engagement
Problem-solving
Critical thinking
Regulatory Compliance
ICH-GCP The National Institute on Drug Abuse (NIDA)
ICH-GCP The National Institute on Drug Abuse (NIDA)