ĐƠN VỊ NGHIÊN CỨU LÂM SÀNG ĐẠI HỌC OXFORD

*


tin tức tuyển chọn dụng Điều păn năn viên Nghiên cứu vớt lâm sàng - Đơn vị phân tích lâm sàng của Đại học Oxford Việt Nam

tin tức tuyển chọn dụng Điều phối hận viên Nghiên cứu lâm sàng - Đơn vị nghiên cứu lâm sàng của Đại học tập Oxford Việt Nam


Phòng baohiemlienviet.com gửi những anh, chị cựu học viên/sinc viên đọc tin ứng tuyển vị trí: Điều pân hận viên Nghiên cứu vớt lâm sàng (Clinical Retìm kiếm Coordinator) - Đơn vị nghiên cứu và phân tích lâm sàng của Đại học Oxford VN (The Oxford University Clinical Retìm kiếm Unit Vietnam - OUCRU)

 

Job summary 

A highly motivated Coordinator is required to work with in our clinical trials unit (CTU) to work with OUCRU’s Principle Investigators (PIs) & local partners to lớn coordinate & manage the implementation of OUCRU research projects across Vietphái mạnh, including both clinical and community-based studies lớn ensure efficient and high chất lượng retìm kiếm operations in line with international standards; to contribute to lớn the continued growth and development of OUCRU’s retìm kiếm portfolio in Vietnam

 

Key tasks và responsibilities

Work with PI’s & local partner retìm kiếm institutions and hospitals lớn finalize retìm kiếm protocols, budgets, và other required documents project start-up phaseSupport PI’s và local partners khổng lồ prepare, submit và get ethical approval from local IRB committee(s) and/or other relevant international EC boardsDevelop standard operating procedures to lớn control the quality of study implementationOrganize logistics of study materials, including consumables, other studies’ materials & documentsClosely supervise the implementation of the studies lớn ensure efficient and high unique retìm kiếm operation in line with international standards, including principles of Good Clinical PracticeTraông xã study progress and identify problems. Report to stakeholders as required & work with PI’s and local partner(s) khổng lồ find solutionsLiaise with sponsor for monitoring/audits. Write, tệp tin & collate trial documentation & visit reports with respect to monitoring.Plan, implement and coordinate all aspects of data collection và entering management and cleaning, and storage, following OUCRU’s data management policy và ICH GCP.. guidelines if appropariateExedễ thương study-related administrative tasks, such as collection of data và regulatory documents, managing reimbursement for patients and study staff, filing or retrieving files, maintaining patient charts và supply inventories with clinical trials.Translate study documents (Vietnamese – English – Vietnamese) if appropriate.Supervise the transfer of documents khổng lồ the central OUCRU tệp tin VPS.Coordinate patient visit schedule in clinical studies as per study protocol where appropriate.Organise, plan and co-ordinate ICH GCPhường training for local study staff in Hanoi và the region whenever needed.Train study staff and investigators in protocol relevant procedures including those for laboratory samples, data collection và recording, medication & patient assessment wherever it is appropriate.Support & participate in training of new CTU staff in OUCRU procedures pertaining to CTU duties.Participate in study team meetings lớn cốt truyện experience và contribute to the knowledge of others in the team.Attend career training lớn improve sầu skills & update relevant knowledge.Other tasks as required.

Bạn đang xem: Đơn vị nghiên cứu lâm sàng đại học oxford

 

Selection criteria

Essential Criteria:

Medical Doctor, Public health, Pharmacy, NurseGood understanding of general ethical considerations applicable to lớn research and good clinical practice (GCP) guidelines & other relevant regulations in conducting studies, including clinical trialsAdvanced level of English comprehension, including the ability to vày translations from English to lớn Vietnamese & vice versaExcellent interpersonal communication/diplomatic skills with people of different backgrounds & social positionsEXCELLENT VIETNAMESE LANGUAGE SKILLS: listening, speaking, reading, writing.

Xem thêm: Giải Hóa 9 Bài 20 Hợp Kim Sắt Gang, Thép, Hóa 9 Bài 20: Hợp Kim Sắt: Gang, Thép

Desirable Criteria:

Master degree in clinical studies, epidemiology and public health or related fieldsExperience of working in a retìm kiếm institution with involvement in research protocol and data collection tools development và IRB submission Experience of monitoring/managing research/studies, including both clinical trials/research and community-based studiesExperience in budgeting, monitoring budget and managing procurement

 

Benefits

Contracted salary: Negotiate (depending on actual experience and education)Optional insurance: In-patient và out-patient medical coverage; Personal accident insurance coverage13th month salary (annual bonus)One month salary for annual clothesAnnual leave sầu 18 days/year (increased to lớn 21 days in year three, 28 days in year four & 30 days from year five).Vietphái nam Social và Health insurance, Siông xã leave sầu, Personal leave sầu, Maternity leave và National holidays will be based on Vietnam giới Labor Law

 

How to apply

Interested candidates are invited lớn sover curriculum vitae, application and copies of relevant certificates by email khổng lồ : trangbh
oucru.org

* The cover letter should detail: 

What part of your education, training or employment history has best equipped you for this position and why you would be a good candidate?What experience have sầu you had of working with communities?Contacts / reference letters of two referees who are your lachạy thử HR, line manager và can provide details of your relevant work experience & responsibility

* Only short-listed applicants will be contacted for interview. Please no telephone contact after submitting the application

Contact person

Ms. Bui Huyen Trang

Deadline for submission: 27th March 2020

 

 

 

Department: OUCRU – HN

Location: This post is based in Hanoi, Viet Nam. There will be a requirement to lớn travel within Viet Nam lớn tư vấn projects, mainly in the northern region, and internationally to lớn attkết thúc conferences.

Hours of work: Full time Monday – Friday, 37.5 hours per week, extra hours may be required.

Tenure: Initially for 01 years, including a 02 month probation period, with possibility of extension based on annual performance appraisal & research approval

Reporting to: Clinical Trial Unit Manager / Director of OUCRU – HN

 

Thông tin cụ thể vui mừng coi tại đây: https://ngorecruitment.org/clinical-research-coordinator-oucru.html?fbclid=IwAR15CJtT8BqZp3ViIpnQo3YMDn_q-cOLJP9vxZmnXz0NHrVnw8r9Z5p3phc