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 18 เม.ย. 2568
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