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Job ID :
61606BR
Location :
China - Suzhou
:
Job Description

Responsibilities:

To perform study setup and provide project management services to clients and ensure all the related procedure in accordance with cGMP.

Perform study setup duties and provide insightful input on project-related documents (essential document collection process, final analysis plan, final study report, etc.) Coordinate information and communications for designated projects and project meetings(internal and external), be active participant and provide post-meeting documentations/minutes; ensure the information and communications in accuracy and the proof documentation in place Monitor the day to day running of designated projected Maintain internal study management databases and project documentation files Independently interact with clients and global team.

Minimum Qualifications:

Education: Bachelor degree, preferred majoring in life science or pharmaceutical related

Years of

Experience: At least 2 years relevant working experience, 1-2 yrs project management experience

will be plus

Knowledge: Project management, clinical trials, logistics

Competency: Coordination, communications, problem-solving, multi-task

Work Schedule: 08:30 AM TO 05:30 PM core hours, additional hours as required.

0-5%Travel

Preferred Qualifications:

Bachelor degree 3 yrs working experience in relevant to coordination and project management Good command of English




Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status.
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