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
Manager/Senior Manager, Global New Product Planning Cambridge, MA

Reporting to the Director of New Product Planning, this position is responsible for developing commercial perspectives for pipeline assets, building revenue forecast and managing product launch preparation projects.

Finance and Strategy
Manager/Senior Manager, Safety Science Cambridge, MA, Emeryville, CA, Ridgefield, NJ, San Mateo, CA

The person in this position collects, analyzes and displays safety data to allow medical interpretation and action concerning potential and actual safety signals with assigned products. This person will assist more senior staff in creating reports and archiving documents.

Pharmacovigilance and Drug Safety
MANAGER/SR. MANAGER, CLINICAL SYSTEMS VALIDATION QA Emeryville, CA, San Mateo, CA

Manager/Sr. Manager of Computer Systems Validation QA will oversee the GxP computerized systems validation and provide QA oversight within BeiGene.  The individual ensures that GxP systems meet intended uses and comply with applicable regulations, current industry practices, and BeiGene’s procedures

Quality Assurance & Control
Medical director, Clinical development Beijing, CN, Shanghai, CN

TBD

Accounting & Finance
Medical Director/Senior Medical Director Safety Science Cambridge, MA, Emeryville, CA, Ridgefield, NJ, San Mateo, CA

Person in this position provides the medical input needed to interpret safety data derived from any source including clinical trials, literature, post marketing studies and post marketing spontaneous adverse event reports in order to identify and evaluate potential safety signals and develop appropriate risk mitigation strategies when a safety signal is confirmed.

Pharmacovigilance and Drug Safety
Project Coordinator San Mateo, CA

BeiGene is a global biopharmaceutical company dedicated to the discovery and development of innovative drug therapies for the treatment of cancer.  We are seeking a dedicated Project Coordinator for our San Mateo, CA office to assist with the planning, coordination and tracking of various projects within our Hematology Portfolio. This role will provide project support in the Program management and other cross functional activities, coordination and reporting of assigned…

Program Management
QA SPECIALIST/ SUPERVISOR Beijing, CN

TBD

Regional Head of PV Asia-Pacific Beijing, CN

The Regional Head will be responsible for the line management of PV personnel in the region who have both local and global roles. The Regional Head will be the PV regulatory expert for the region and the chief PV contact person for the regulatory authorities in the region for investigational and marketed products.

Pharmacovigilance and Drug Safety
RESEARCH INVESTIGATOR/ SENIOR RESEARCH INVESTIGATOR – PRECLINICAL TUMOR IMMUNOLOGY Beijing, CN

BeiGene (Beijing) is searching for an investigator in the field of tumor immunology to provide expertise in developing our immuno-oncology pipelines. This individual will design and execute proof of concept studies in pre-clinical models of tumor immunology, and assist in cross-functional development of our research strategy.

Senior Analyst, Clinical Analytics Remote

Responsible for developing clinical analytics solutions globally with a focus on the TIBCO Spotfire platform. Analytics projects will primarily be aimed at clinical data review, risk-based monitoring, clinical safety, and dashboarding.

Biometrics
Senior Business Analyst, Veeva Center of Excellence Cambridge, MA, Emeryville, CA, Ridgefield, NJ, San Mateo, CA

As part of BeiGene’s Global Enterprise Applications team, the Senior Business Analyst, Veeva Center of Excellence, will be responsible for implementation and management of BeiGene’s Veeva application ecosystem to meet regulatory requirements and business needs.

The ideal candidate should bring experience working in Veeva environments with the ability to manage multiple projects across different functions.  The candidate should also be experienced at running IT projects as a business…

Information Technology
Senior Clinical Database Programmer Cambridge, MA

The clinical Database Programmer is responsible for all technical aspects of study build, validation, and maintenance, including clinical programming activities for new and ongoing clinical studies, start-up activities, database revisions, timely resolution of technical issues related to the conduct and closeout of clinical studies. Database Programmer works collaboratively with Data Management and multiple functional groups to complete programming tasks per agreed upon timelines.

Clinical Informatics
Senior Clinical Database QA Engineer Cambridge, MA

Clinical database QA engineer is responsible for all QA aspects of study build, validation, and maintenance, including QC activities for new and ongoing clinical studies, start-up activities, database revisions, timely resolution of technical issues related to the conduct and closeout of clinical studies. Lead clinical database QA Engineer works collaboratively with Clinical Informatics, Data Management and multiple functional groups to complete QC tasks per agreed upon timelines.

Clinical Informatics
Senior Clinical Research Associate (SCRA) Cambridge, MA, Emeryville, CA, Ridgefield, NJ, San Mateo, CA

The CRA performs monitoring activities related to initiation, conduct (recruitment, quality data collection) and timely completion of Oncology and Pharma clinical trials within the country.

The CRA is responsible to deliver data within timelines and required quality standard, responsible for adherence to monitoring procedures in accordance with GCP and ICH, local regulations and SOPs.

Clinical Operations
Senior Clinical Study Manager (SCSM) Cambridge, MA, Emeryville, CA, San Mateo, CA
  • Responsible for the planning, implementation and conduct of large, global, complex oncology clinical trials in Phase I-IV; or multiple smaller early-phase studies. 
  • Provides leadership within the department and makes recommendations with regards to the operational aspects of executing clinical development deliverables.   
Clinical Operations

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

Accept