

Detail-oriented and GCP-certified Study Coordinator with hands-on experience managing clinical trial activities across multiple therapeutic areas, including oncology and infectious diseases. Proven ability to coordinate with investigators, ensure protocol compliance, and maintain high-quality documentation. Skilled in patient recruitment, data entry, and communication with CROs and sponsors.
Understanding of clinical trial processes and workflows
Familiarity with key documents such as protocols, ICFs, CRFs, and SAE reports
Basic knowledge of Good Clinical Practice (GCP) and research ethics
Coordinate effectively with physicians, nurses, patients, CROs, and sponsors
Manage subject scheduling, follow-up visits, lab tests, and other study procedures
Prepare patients and required documentation for study participation
Maintain accurate and complete study records and source documents
Complete paper or electronic Case Report Forms (CRFs)
Track informed consent and report adverse events (AEs/SAEs)
Explain study information clearly to patients during the informed consent process
Communicate effectively with sponsors and Clinical Research Associates (CRAs)
Write professional emails and study-related reports
Ability to read and understand clinical trial documents in English
Communicate with sponsors/CROs in a professional manner
Write and respond to emails or reports in English
Verify the accuracy of patient data and study documentation
Prevent errors that may affect the quality or ethics of the study
Work effectively under tight timelines
Handle multiple tasks and priorities under pressure
Study design