Join Us in the Fight Against Cancer

Join Us in the Fight
Against Cancer

BeiGene continues to grow at a rapid pace with challenging and exciting opportunities for experienced professionals. When considering candidates, we look for scientific and business professionals who are highly motivated, collaborative, and most importantly, share our passionate interest in fighting cancer.

Current Openings in China

79 jobs found
Openings Location Job Summary Department
Sr. Manager, AD, Biostatistics Emeryville, CA, Ridgefield, NJ, San Mateo, CA


Essential Functions of the job:

·       A minimum of a Master Degree with 8+ years of experience or a PhD in Statistics or related field with  4+ years of experience in clinical drug development is required.

·       Knowledge of SAS and/or R is strongly desirable.

·       Experience with clinical trials and knowledge of regulatory guidance are required.

·       Hematology experience is preferred but not required.

·      …

Submissions Operations Management Sr. Manager, Reg Ops Emeryville, CA, San Mateo, CA

The Submissions Operations Manager is responsible for providing publishing, technical editing and general submission support to the growing Regulatory Operations team.  This person will help to establish the Submission Operation Management Function at BeiGene and help to establish an approach for regulatory submissions.

This position will provide global support to Regulatory Affairs with an immediate focus on work on submissions for China and the US.  This person will collaborate…

Regulatory Operations
System and Application Support Analyst Emeryville, CA

Reporting to the Director, IT Operations, System and Application support analyst will be responsible for optimizing employee productivity by effectively managing and supporting enterprise infrastructure applications and services under the Infrastructure & Operations team.

Information Technology
Vice President, Regulatory Affairs US/EU Cambridge, MA, Emeryville, CA, Ridgefield, NJ, San Mateo, CA

The Vice President, Regulatory Affairs will be responsible for developing, implementing, and advising on US/EU regulatory strategies for development programs to secure and maintain market access for product(s) in line with business objectives, and in coordination with key internal stakeholders. 

Regulatory Affairs

This website uses cookies to improve your overall experience. With your continued use, you are agreeing to accept our use of cookies.