Recru it Manager / Head Of Hanoi Clinical Trials Unit (Jdhan_0621_009) tại Đống Đa
Oxford University Clinical Research Unit
Địa điểm làm việc: Hà Nội
Hết hạn: 30/09/2021
- Chi tiết công việc
- Giới thiệu công ty
Vị trí công việc này hiện tại đã hết hạn nộp hồ sơ, bạn có thể tham khảo thêm một số công việc tương tự tại đây:
Mô tả công việc
The post-holder must be pro-active and ensure the work is of high standard. The selected candidate is expected to
· Supervise, guide, and advise a growing team of clinical research coordinators and administrators.
· Supervise other non-CTU staff responsible for coordinating and monitoring OUCRU studies.
· Support processes of regulatory compliance and response to operational issues.
· Ensure research studies are performed with integrity and high standard by providing optimal staffing and collaborating with the clinical and non-clinical support services departments.
· Ensure compliance to clinical research best practices, all applicable federal, state, and institutional regulatory guidelines.
· Perform assessments and evaluations to determine needs and best approaches to implementation of new processes, protocols, and procedures.
· Facilitate and ensure cross-functional resource support for projects.
· Work with OUCRU Hanoi Admin and Finance in the development of project agreement and other research related contracts.
· Work with OUCRU Hanoi Admin and Finance, researchers and collaborators to solve all issues related to study budgets and payments.
· Maintain an up-to-date understanding of the applicable trial regulations, both local and international, transfer to investigators on regulatory changes and ensure that these standards are implemented in all OUCRU HN research.
· Lead or support execution of new research projects as project coordinator
· Ensure and maintain consistency with OUCRU programme-wide procedures regarding study operations and governance by frequent liaising with OUCRU-HCMC.
· Act as focal point in liaison with regulators, ethical committees and CTU OUCRU-HCMC to ensure optimal communications between OUCRU and these bodies.
· Build relationships and maintain good and frequent communication with collaborating staff at study sites, to ensure participants' well-being, compliance with study protocols and quality of clinical data.
· Build and maintain relationships with points-of-contact / leadership at study sites and act as a liaison between OUCRU Hanoi and the site.
· Develop and retain research staff providing them an environment that fosters professional development through continuous learning.
· Other tasks as required
· Supervise, guide, and advise a growing team of clinical research coordinators and administrators.
· Supervise other non-CTU staff responsible for coordinating and monitoring OUCRU studies.
· Support processes of regulatory compliance and response to operational issues.
· Ensure research studies are performed with integrity and high standard by providing optimal staffing and collaborating with the clinical and non-clinical support services departments.
· Ensure compliance to clinical research best practices, all applicable federal, state, and institutional regulatory guidelines.
· Perform assessments and evaluations to determine needs and best approaches to implementation of new processes, protocols, and procedures.
· Facilitate and ensure cross-functional resource support for projects.
· Work with OUCRU Hanoi Admin and Finance in the development of project agreement and other research related contracts.
· Work with OUCRU Hanoi Admin and Finance, researchers and collaborators to solve all issues related to study budgets and payments.
· Maintain an up-to-date understanding of the applicable trial regulations, both local and international, transfer to investigators on regulatory changes and ensure that these standards are implemented in all OUCRU HN research.
· Lead or support execution of new research projects as project coordinator
· Ensure and maintain consistency with OUCRU programme-wide procedures regarding study operations and governance by frequent liaising with OUCRU-HCMC.
· Act as focal point in liaison with regulators, ethical committees and CTU OUCRU-HCMC to ensure optimal communications between OUCRU and these bodies.
· Build relationships and maintain good and frequent communication with collaborating staff at study sites, to ensure participants' well-being, compliance with study protocols and quality of clinical data.
· Build and maintain relationships with points-of-contact / leadership at study sites and act as a liaison between OUCRU Hanoi and the site.
· Develop and retain research staff providing them an environment that fosters professional development through continuous learning.
· Other tasks as required
Yêu cầu
Selection criteria
Essential Criteria:
· Medical doctor or Master's degree in a health-related science with at least 3 years of relevant experience conducting or managing clinical trials.
· Excellent Vietnamese and very good English language skills
· 2-4 years of people management experience
· Good understanding of Good Clinical Practice guidelines in clinical research
· Excellent skills in oral and written communication
· Ability to work closely with other study staff, hospital and public health/government collaborators
· Good attention to detail in following protocols and keeping records
· Interest in clinical and/or epidemiological research
· Willing to travel within country and abroad
Desirable Criteria:
· Experience in working in an international environment
· Experience in liaising with Ministries and/or other national bodies
· Understanding of academic, research or not-for-profit working environment
· Able to work with a minimum of supervision
Essential Criteria:
· Medical doctor or Master's degree in a health-related science with at least 3 years of relevant experience conducting or managing clinical trials.
· Excellent Vietnamese and very good English language skills
· 2-4 years of people management experience
· Good understanding of Good Clinical Practice guidelines in clinical research
· Excellent skills in oral and written communication
· Ability to work closely with other study staff, hospital and public health/government collaborators
· Good attention to detail in following protocols and keeping records
· Interest in clinical and/or epidemiological research
· Willing to travel within country and abroad
Desirable Criteria:
· Experience in working in an international environment
· Experience in liaising with Ministries and/or other national bodies
· Understanding of academic, research or not-for-profit working environment
· Able to work with a minimum of supervision
Quyền lợi
- Company trip once a year + Joining party
- Bonus by individual ability and company's performance.
- Salary and position is reviewed 1 time a year
- Having chances to get attractive company bonus every month/year
- Social insurance, health insurance, unemployment insurance and other benefits
- Dynamic and sociable working environment.
- Bonus by individual ability and company's performance.
- Salary and position is reviewed 1 time a year
- Having chances to get attractive company bonus every month/year
- Social insurance, health insurance, unemployment insurance and other benefits
- Dynamic and sociable working environment.
Thông tin khác
Mức lương:
Thỏa thuận
Địa điểm:
Đống Đa
, Hà Nội
Hạn nộp hồ sơ:30-09-2021
Chức vụ:Nhân viên
Hình thức:Toàn thời gian
Ngành nghề:Y Tế
Thỏa thuận
Địa điểm:
Đống Đa
, Hà Nội
Hạn nộp hồ sơ:30-09-2021
Chức vụ:Nhân viên
Hình thức:Toàn thời gian
Ngành nghề:Y Tế
Thông tin chung
- Ngày hết hạn: 30/09/2021
- Thu nhập: Thỏa thuận
Giới thiệu công ty
Xem trang công ty
Our ten-year vision is to have local, regional and global impact on health by leading aOur ten-year vision is to have local, regional and global impact on health by leading a locally driven research programme on infectious diseases in Southeast Asia. locally driven research programme on infectious diseases in Southeast Asia.
Our ten-year vision is to have local, regional and global impact on health by leading aOur ten-year vision is to have local, regional and global impact on health by leading a locally driven research programme on infectious diseases in Southeast Asia. locally driven research programme on infectious diseases in Southeast Asia.
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