ค้นหา :

patients หางานpatients

สมัครงานpatients งานpatients

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 patient’s 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; อัตรา 2 เงินเดือน ไม่ระบุ ศูนย์ประสานความร่วมมือระหว่างไทย-ออสเตรเลีย-เนเธอร์แลนด์ เพื่อการศึกษาวิจัยทางคลินิกด้านโรคเอดส์ จังหวัด กรุงเทพมหานคร ปทุมวัน วันที่ 15 มี.ค. 2567

ผู้ช่วยพยาบาลวิจัย • Prepare patients schedules included, lab requests, CRFs, OPD and other • 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. • Have a thorough knowledge of any study protocol (including amendments) that you are assigned to. • Perform visits in accordance with the protocol; • Co-ordinate their daily schedule with the requirements of the patients according to the protocol. • Provide direct patient care, using expert nursing knowledge, to their assigned patient caseload. • 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. • Review as soon as practicable the results of diagnostic tests and to file results in patient’s clinical notes record. • inform the patient of results as required for patient safety and in accordance with the protocol and the requirements of GCP. อัตรา 3 เงินเดือน Attractive salary ศูนย์ประสานความร่วมมือระหว่างไทย-ออสเตรเลีย-เนเธอร์แลนด์ เพื่อการศึกษาวิจัยทางคลินิกด้านโรคเอดส์ จังหวัด กรุงเทพมหานคร ปทุมวัน วันที่ 14 มี.ค. 2567

Customer Service Supervisor (สาขา รพ.กรุงเทพ พัทยา) • To adhere to SODEXO WAY Service Standards • To co-ordinate with all department of operation in ensuring highest customer satisfaction is provided by tailoring service and products to individuals or special needs • To resolve satisfaction shortfall with patients and hospital staff and ensuring corrective actions are taken • To conduct satisfaction survey and take corrective action when customer’s expectations are not met • To actively detect potential problems and take proactive actions in ensuring highest customer satisfaction • To build a positive and constructive relation with ward staff to ensure open and effective communication is maintained or improved • To act as an interpreter when required • To carry out any other tasks as required by immediate supervisor. อัตรา หลายอัตรา เงินเดือน N/A บริษัท โซเด็กซ์โซ่ เฮ็ลธแคร์ ซัพพอร์ท เซอร์วิส (ประเทศไทย) จำกัด จังหวัด ชลบุรี วันที่ 13 มี.ค. 2567

Clinical Research Associate 1) Oversees the planning, scheduling, and carrying out of clinical activities and procedures, ensuring efficient workflow and adequate care and treatment of research subjects. And ensures that all clinical activities are carried out in accordance with established research protocol and standards and in compliance with all applicable laws, regulations, policies, and procedural requirements. 2) Coordinates, plans, and implements as protocol requirement for the study; monitors study activity and prepares reports to sponsors and investigators as appropriate. 3) Plans and coordinates the initiation of research study protocol, and implements, and maintains data collection and analysis systems in support of research protocol; may coordinate the collection and analysis of research data. 4) Monitors the progress of research activities; develops and maintains records of research activities, and prepares periodic and ad hoc reports, as required by investigators, administrators, funding agencies, and/or regulatory bodies. 5) Interview patients for clinical trial and collects and analyses data to validate eligibility and patient commitment 6) Obtains pre-screening medical documents by communicating with appropriate sources 7) Educates patients about the clinical trial and their roles in the protocols and any other vital information 8) Provides patients with documentation validating their study participation as needed 9) Acts as a liaison between patients and physicians 10) Prepares and maintains manual and computerized data in patient study books according to prescribed standards 11) Transcribes data in case report from books อัตรา 1 เงินเดือน attractive salary ศูนย์ประสานความร่วมมือระหว่างไทย-ออสเตรเลีย-เนเธอร์แลนด์ เพื่อการศึกษาวิจัยทางคลินิกด้านโรคเอดส์ จังหวัด กรุงเทพมหานคร ปทุมวัน วันที่ 13 มี.ค. 2567

Clinical Research Associate 1) Oversees the planning, scheduling, and carrying out of clinical activities and procedures, ensuring efficient workflow and adequate care and treatment of research subjects. And ensures that all clinical activities are carried out in accordance with established research protocol and standards and in compliance with all applicable laws, regulations, policies, and procedural requirements. 2) Coordinates, plans, and implements as protocol requirement for the study; monitors study activity and prepares reports to sponsors and investigators as appropriate. 3) Plans and coordinates the initiation of research study protocol, and implements, and maintains data collection and analysis systems in support of research protocol; may coordinate the collection and analysis of research data. 4) Monitors the progress of research activities; develops and maintains records of research activities, and prepares periodic and ad hoc reports, as required by investigators, administrators, funding agencies, and/or regulatory bodies. 5) Interview patients for clinical trial and collects and analyses data to validate eligibility and patient commitment 6) Obtains pre-screening medical documents by communicating with appropriate sources 7) Educates patients about the clinical trial and their roles in the protocols and any other vital information 8) Provides patients with documentation validating their study participation as needed 9) Acts as a liaison between patients and physicians 10) Prepares and maintains manual and computerized data in patient study books according to prescribed standards 11) Transcribes data in case report from books อัตรา 1 เงินเดือน attractive salary ศูนย์ประสานความร่วมมือระหว่างไทย-ออสเตรเลีย-เนเธอร์แลนด์ เพื่อการศึกษาวิจัยทางคลินิกด้านโรคเอดส์ จังหวัด กรุงเทพมหานคร ปทุมวัน วันที่ 7 มี.ค. 2567

เภสัชกร This position is responsible for managing clinical data from clinical research studies conducted by the Pharmacy Division. Specific responsibilities include: • provide pharmacy services, Help in the development of guideline, protocols for patient group discussions • Support the clinical trials’ personnel, especially by providing information about the correct formulations and doses of medicines. • Assist nursing personnel with patient counselling for patient adherence especially with information related to pharmaceuticals. • Provide appropriate and accurate information for patients about the dispensed medications, doses and possible side effects • Calculate amounts of drugs required for budgeting and ordering • Other duties as assigned อัตรา 2 เงินเดือน N/A ศูนย์ประสานความร่วมมือระหว่างไทย-ออสเตรเลีย-เนเธอร์แลนด์ เพื่อการศึกษาวิจัยทางคลินิกด้านโรคเอดส์ จังหวัด กรุงเทพมหานคร ปทุมวัน วันที่ 3 มี.ค. 2567

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 patient’s 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; อัตรา 3 เงินเดือน attractive salary ศูนย์ประสานความร่วมมือระหว่างไทย-ออสเตรเลีย-เนเธอร์แลนด์ เพื่อการศึกษาวิจัยทางคลินิกด้านโรคเอดส์ จังหวัด กรุงเทพมหานคร ปทุมวัน วันที่ 26 ก.พ. 2567