崗位職責(zé):
1.Run the project according to the existing SOP.
2.Ability to create SOPs in accordance with CAP, CLIA regulations.
3.Preparation of manuals for clinical trial projects.
4.Project-related training (online or on-site).
5.Coordinate the communication between the project team and customers, and respond to customer questions in a timely manner.
6. Maintain project-related documents and records.
7. Supervise the operation of the project and discover and deal with problems in time.
8.Coordinate the transfer, testing and reporting of samples.
9. Prepare project phase/summary report or PPT.
10. Assist internal and external audit.
11. Other tasks arranged by the supervisor.
任職要求:
1.Ensure smooth operations of projects;
2.Coordinate and communicate project status internally and externally;
3.Oversee development and maintenance of all project management-related documentation;
4.Monitor the progress of clinical trials, conduct risk management and control of the project as a whole, and proactively predict possible problems in the project;
5.Coordinate specimen testing, transfer and reporting with clients;
6.Follow up customer contract signing with sales;
7.Assist and coordinate internal and external audit.
Core business/Functional skills and education requirements:
What is the critical experience, training skills, education, or capabilities?
1.Must have earned a bachelor
s degree or above in a medical technology, chemical, physical, biological biotechnical or clinical laboratory science, or medical technology from an accredited institution.
2.Strong skills, both written and verbal, outstanding interpersonal skill are essential job requirement. Strong English written skill is a must, and verbal skill is a bonus.
3.Must be able to openly share information and work in a team-oriented manner in order to accomplish performance objectives.
4.Proactive, strong sense of responsibility, Good team work spirit and communication skills.
5.Familiar with computer software for Office, excel, etc.