Clinical Trial Reg Affairs Specialist III

Posted on October 7, 2025

|
1 min read
|
Views

Job details

  • Profession: Uncatalogued Profession

  • Country of the Job: China

  • State of the Job: CHN

  • City of the Job: Beijing

  • Job Application Deadline (Year): 2025

  • Type of job: Not specified. See Job Description

  • Hiring Company: ThermoFisher Scientific

  • Mode of Work: Onsite

  • Applier's country: China

  • Benefits Included: Disability protection, Education

Work Schedule

Standard (Mon-Fri)

Environmental Conditions

Office

Job Description

Responsibilities:

Be responsible for the registrations of imported drug. Including but not limited to the good communications with NMPA, CDE and other authority, registration documents preparation, performing the test, documents submissions and follow up of NMPA until get the approval. Timely documents archiving. Other tasks if needed.

Minimum Qualifications: Bachelor degree

At least 2-3 years’ experience on imported drug registration

Good at written and oral English

Preferred Qualifications: Medical education background

The experience on all of API, ANDA, IND and other type registration is preferred

Good communications skills

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.