Cui Chen Email & Phone Number

China

Identified investigators for projects.Prepared and submitted dossiers for Ethics Committee and collect regulatory documents.Conducted meetings for initiation and trial closure.Trained site staff on project-specific issuesEnsured protocol compliance, ICH-GCP and other regulatory obligations at trial sites Performed monitoring activities, which includes verifies the accuracy and authenticity of clinical data, manage investigational products and other trial related supplies, maintain adequate clinical trial documentation etc.Ensure the timely reporting of study information, which includes safety reporting t relevant study team member and regulatory authorities.Managed quality dataPrepared monitoring reports

Identified investigators for projects.Prepared and submitted dossiers for Ethics Committee and collect regulatory documents. Conducted meetings for initiation and trial closure.Trained site staff on project-specific issuesEnsured protocol compliance, ICH-GCP and other regulatory obligations at trial sites Performed monitoring activities, which includes verifies the accuracy and authenticity of clinical data, manage investigational products and other trial related supplies, maintain adequate clinical trial documentation etc.Ensure the timely reporting of study information, which includes safety reporting t relevant study team member and regulatory authorities.Managed quality dataPrepared monitoring reports

Based on the patient's symptoms make diagnosis.Made the corresponding treatment scheme.Written the Medical records.Reported the patients’ conditions and treatment schemes to attending doctor and chief.Gave patients health guidance when they discharge from hospital.

Beijing City, China

Based on the patient's symptoms make diagnosis.Made the corresponding treatment scheme.Written the medical records.Reported the patients’ conditions and treatment schemes to attending doctor and chief.Gave patients health guidance when they discharge from hospital