| พยาบาลวิจัย |
1. Explain the protocol to the patient according to the information sheet, especially known data about the study medication, standard treatment, research goals, status of patients disease, disease progression and implications of progression, leading to the patient being able to sign the informed consent;
2. Identify patients suitable for a specific clinical trial through clinical notes searches, database searches and referrals from consultants and other physicians, and maintain accurate and up-to-date logs of patients potentially eligible for clinical trials; and perform visits in accordance with the protocol;
3. Provide direct patient care, using expert nursing knowledge, to their assigned patient caseload;
4. Assess the patient, so as to plan, intervene and follow-up on any sign or symptom, whether HIV-related or not, to maintain the rights and well-being of the patient and to fulfil the requirements of the protocol;
5. Inform the patient of results as required for patient safety and in accordance with the protocol and the requirements of GCP;
6. Report any adverse events or serious adverse events to the responsible trial physician as soon as practicable and to co-ordinate the management of the event;
7. Assist as required in procedures performed by physicians, especially but not limited to blood collection and intravenous catheter placement, pharmacokinetic procedures, intradermal skin testing, and other procedures that may be required in an expert and professional way, always practising universal precautions;
8. Collect and accurately record data in the Case Report Form (CRF), in accordance with the protocol and the requirements of GCP, and to make corrections as necessary in the appropriate manner; |
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