According to the needs of individual plan, write the subject recruitment plan
Assist in recruiting and screening subjects
Assist the test host to inform the subjects of the test plan process and assist in obtaining the consent form of the subjects
Implement the clinical trial plan and ensure that the trial process conforms to the guidelines for good clinical trials of drugs
Assist relevant personnel participating in clinical trials to familiarize themselves with the trial plan and the trial process
Prepare documents required for clinical trials
Planning standard operating procedures
Establish a good interactive relationship and communication channel between the test client and the test plan host
Provide medication instruction and care tracking services for subjects
Management and storage of research drugs
Assist in completing the case report form correctly
Filing and preservation of research data related to clinical trials
Treatment of adverse events of subjects
Provide the documents required by the monitor for monitoring
Assist the monitor to prepare the test audit documents
Maintain good doctor-patient relationship
Provide 24-hour round the clock service telephone for subjects
Appointment management of clinical trial personnel
Assist the gcrc/ctc of each hospital to tailor the required clinical resource management services
Good clinical practice
Training and other services related to clinical trial research
