- Facilitate and coordinate the daily clinical trial activities and provide technical support for y physicians, nurses, project assistants and receptionists. Ensure that clinical researches are conducted in accordance with Good Clinical Practice and study.
- Protocols.
- Perform monitoring activities daily to ensure clinical activities comply with protocols, GCP, Vietnam laws and regulations; including but not limited to review of informed consent, paper CRFs, lab results, visit window.
- Conduct study visits: consent process, physical exam, study medication administration, interviewing & counselling.
- Ensure that all protocol specific clinical events are properly reported to CMC. Serious adverse events are proper documented and reported on DAERS in timely manner.
- Provide training & coaching for physicians, nurses, receptionist and project assistants.
- Maintain detailed records of studies as per DAIDS requirements.
- Liaise with other members and components to ensure all protocols are followed and that there is timely documentation and submission of study data.
- Ensure that necessary supplies and equipment for clinic are in stock and in working order.
- Be a role model, share best practices and make recommendations for continuous quality improvement on clinical activities.
- Perform other duties as requested.
- Possess a MD degree
- Good command of English
- Excellent organizational and interpersonal skills
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Việc làm tại các tổ chức phi chính phủ - NGO Recruitment
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- Youtube: http://bit.ly/Youtube_NGORecruitment
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