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
Senior Director, Quality Product Lead and Quality & Business Process Owner San Mateo, CA

Essential Functions of the job:

  • Manage quality related issues impacting the product (technical) to all relevant Quality (China Quality Operations, BeiGene’s internal manufacturing sites in SZ, GZ, BJ, External Quality).  Interface with stakeholders including Quality, CMC, Alliance Partners & CMOs to ensure production, testing and release, and regulatory…
Quality Assurance & Control
Senior Director, Statistical Programming and Clinical Informatics Emeryville, CA

Essential Functions of the job:

  • Leads the Statistical Programming function for BeiGene, and provides strategic, technical and operational leadership for Statistical Programming support for all clinical development programs spanning all phases of development including regulatory submissions.
Statistical Programming
Senior Manager or Associate Director, Inspection Management Emeryville, CA, San Mateo, CA

The Senior Manager or Associate Director of Inspection Management will be based in San Mateo or Emeryville, CA.  This will be a hands-on position that will be responsible for the organization, planning, process and logistics of all health authority inspections. This will include, but not limited to, inspection readiness activities, inspection management training, developing and maintaining BeiGene’s inspection management process and development of inspection management tools and systems.

Quality Assurance & Control
Senior Manager, Biostatistics Emeryville, CA, San Mateo, CA

Supporting the BTK-3111 clinical development with a focus on hematology area, the position will provide high quality statistical support to assigned projects/studies with support of senior staff as necessary.  He/she will work with cross-functional study/project teams in reviewing the data, developing and implementing the statistical analysis plan for CSR and other HA submission document such as clinical summary, providing contents for manuscript/presentation and providing other statistical…

Accounting & Finance
Senior Manager, Case Review Management Emeryville, CA, San Mateo, CA

Person in this position provides the management for medical case review of Individual Case Safety Report (ICSR) from any source, including case load distribution and workflow monitoring in Argus safety database; in addition, develops investigator/study site orientated education curriculum and training materials for SAE reporting, conducts trainings and monitoring progress in SAE report qualities, and perform SAE query analysis.

Pharmacovigilance and Drug Safety
Senior Manager, Statistical Programming Beijing, CN, Shanghai, CN

The Senior Manager, Statistical Programming will work in BeiGene’s Statistical Programming group to manage and support Statistical Programming deliverables for multiple clinical studies.

Biometrics
SENIOR MANAGER/MANAGER, GCP QUALITY ASSURANCE Emeryville, CA, San Mateo, CA

The Manager of GCP Quality Assurance is responsible for implementing and maintaining a balanced, proactive, and phase appropriate approach to GCP Quality Assurance. This position will be primarily responsible for ensuring research and development activities are conducted in accordance with applicable regulatory requirements, guidelines, laws and internally established standards and practices.

Quality Assurance & Control
Senior Manager/Manager, Regulatory Affairs Emeryville, CA, San Mateo, CA

The Manager/Senior Manager, Regulatory Affairs will manage, evaluate, and complete regulatory projects consistent with company goals.  This individual will be responsible for timely planning and coordination of regulatory submissions and provide guidance to cross-functional teams on regulatory strategy and tactics. The Manager will represent Regulatory Affairs on cross-functional project teams, will provide input to the project team, will lead authoring and preparation of annual reporting,…

Regulatory Affairs
Senior Medical Writer/Medical Writer Remote, Emeryville, CA, San Mateo, CA

The Senior Medical Writer is responsible for writing, editing, and formatting clinical regulatory documents that conform to domestic and/or international regulatory submission and internal document standards, while meeting project timelines. Clinical regulatory documents include, but are not limited to, study reports, clinical study protocols or amendments, investigator brochures, regulatory briefing documents, and clinical sections of INDs, NDAs, MAAs and other regulatory submission…

Market Access
Senior Scientist in Biologics- Antibody generation Beijing, CN

Biologics department of BeiGene is dedicated to the discovery and development of novel therapeutic monoclonal antibodies for oncology indications. We are seeking senior scientist who have M.S. training in antibody technology or B.S. with antibody-related experience to support cancer drug discovery.

百济神州(北京)生物科技有限公司生物药部门致力于研究发现具有创新性的抗肿瘤单克隆抗体药物。目前我们需招聘具有抗体技术研究背景的理科硕士或有相关工作经验的理科学士。

Senior Talent Management Analyst Emeryville, CA, San Mateo, CA

The Senior TM Analyst is key to the management of people, processes and data. The Senior TM Analyst is a critical asset in the flow of information and process necessary to recruit, hire, and onboard new employees at BeiGene.  The Senior TM Analyst supports the HR team by participating in the design and management of the workflows supporting Learning and Development, Talent Acquisition, Business Partners activities, and other HR programs as implemented (e.g. Awards).

Human Resources
Senior/Clinical Research Associate (Sr CRA/CRA) Cambridge, MA, Emeryville, CA, Ridgefield, NJ, San Mateo, CA

The CRA executes clinical trial protocols at clinical trial sites and monitors clinical trials in accordance to ICH guidelines and GCP, local regulations, and applicable SOPs. Performs monitoring activities related to initiation, conduct (recruitment, quality data collection) and timely completion of Oncology and Pharma clinical trials within the assigned region.

The CRA is responsible for performing quality oversight site visits and collaborating closely with the Clinical Operations…

Clinical Operations
Senior/Regulatory Affairs Associate Emeryville, CA, San Mateo, CA

BeiGene is seeking an experienced and energetic person to manage, evaluate, and complete regulatory projects consistent with company goals. This individual will be responsible for timely planning and coordination of regulatory submissions and provide guidance to cross-functional teams on regulatory strategy and tactics. The Sr. Associate will assist the Regulatory Affairs team member on cross-functional project teams and will assist on authoring and preparation of annual reporting, and will…

Regulatory Affairs
Specialist, Clinical Start Up Beijing, CN, Shanghai, CN

Accountable for the study start-up timelines and delivery, with high quality and according to ICH/GCP

Clinical Operations
Sr. Manager Data Disclosure and Transparency Emeryville, CA, San Mateo, CA

We have an exciting opportunity within our Regulatory Operations team for a Senior Manager who will be responsible for Clinical Trial Disclosure and Data Transparency Activities.  These activities include coordinating disclosure, transparency and data sharing communication and outreach plans, monitoring the landscape to ensure that BeiGene’s data transparency policy is up to date, and creating key performance indication (KPI) reports that demonstrate adherence to regulations.  This person…

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

Accept