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Code: C6184
临床项目经理(Clinical Project Management)
This is a regular Job Posting
Employer: 上海赛笠生物科技有限公司
Working Place: Singapore
Office Address: 上海市浦东新区紫萍路908弄
Job Type: Full Time
Industry & Field: Biotechnology
Vacancies: 1
Salary: Monthly Salary: RMB (CNY) 40,000 to 50,000
Phone Number: 15800954358
Contact Name: 刘耀烛
Refresh Date: Sep. 5, 2023
Expiration Date: Sep. 24, 2023     Expired
Job Description: 
- Develop and manage project plans, including timelines, budgets, and resource allocation
- Coordinate and oversee activities of cross-functional project teams, including investigators, Contract Research Organizations (CROs), and other external vendors
- Ensure all clinical trials are conducted in accordance with relevant regulations, guidelines, and Standard Operating Procedures (SOPs)
- Regularly communicate with internal and external stakeholders, providing project status updates and addressing any issues or concerns
- Monitor and track project progress, identify risks and issues, and implement corrective actions as necessary
- Prepare and maintain study documents, including study protocols, informed consent forms, and case report forms
- Manage clinical trial budgets, including tracking and reporting expenses, and ensuring projects are completed within budget
- Participate in the selection and oversight of external service providers, such as central laboratories and data management companies
- Work with the study team to ensure research sites are adequately trained and equipped to conduct clinical trials
- Support the preparation and submission of regulatory documents, such as Investigational New Drug (IND) applications and Institutional Review Board (IRB) approvals
- Stay current with industry trends, regulations, and best practices in clinical research management.
Qualifications & Requirements: 


1. Bachelor's degree or above in medicine, pharmacy, biology, or related fields.
2. Minimum of 1 year of clinical project management or related experience, with preference given to those with clinical project management experience at a CRO company.
3. Familiar with relevant regulations and standards in clinical research, including GLP and GCP.
4. Excellent communication skills and teamwork spirit, able to effectively coordinate and manage project teams.
5. Strong problem-solving and decision-making abilities, able to handle various challenges and difficulties in the project.
6. Strong planning and organizational skills, able to work according to predetermined goals and timelines.
7. Strong learning and adaptability, able to continuously learn and update professional knowledge.
8. Strong English reading and writing skills, able to effectively communicate and collaborate with foreign teams and collaborators.
Benefits & Welfare: 
1. Provide competitive salary and benefits;

2. Provide good career development opportunities and promotion space;

3. Provide travel and training opportunities at home and abroad;

4. Provide excellent working environment and team atmosphere.
Employer Introduction: 

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Address: Unit 403, ZhongLian Building, No.88(A), Anwai Avenue, Dongcheng District, Beijing 100011 China
Telephone: 400-780-1070    (Office) 010-64217250  021-61900630  0755-66810935     Fax: 010-64217809
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