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At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections, where you are valued, accepted and respected for who you are,
JOB REQUIREMENTS Academic / Professional Qualification MSc/PhD in Statistics, Mathematics, or other related data science majors Knowledge of the technical and regulatory requirements related to the role Experience of regulatory interactions and/or submissions Technical / Skills
Typical Accountabilities: - Support Global Study Leaders (GSL) and Global Study Associate Manager (GSAM) by completing delegated study work. - Initiate and lead the set-up of the electronic Trial Master File (eTMF). Maintain and close the
岗位主要职责Responsibilities : 建立与国家医保相关部门的合作关系； 管理与医保局相关项目合作，包括项目前期准备、内外部沟通、项目跟进与结题等工作 具有良好的沟通能力及高层次客户的管理能力； 具有良好的团队合作能力； 具有国家相关政策收集、学习及理解能力； 具有项目管理能力，在项目合作、会议开展中预防不良突发事件的产生。 要求Qualifications: 医学相关专业学士及以上学位 五年以上相关工作经验. 熟悉政府事务工作的具体工作流程. 必须具备在医药行业中销售工作的经验 具备医药行业内市场准入工作经验优先 具备强有力的分析能力和统筹计划能力 具有团队合作精神 Date Posted05-Jun-2026 Closing Date26-Jul-2026 AstraZeneca embraces diversity and equality of opportunity. We are committed to building an inclusive and diverse
The Clinical Operations Program Lead plays a pivotal role to provide input to optimize trial execution, coordinate governance interactions and product strategy. This role maintains accountable to the Global & China Project Team (GPT/CNPT) for oversight
Introduction to role The Site Operations Lead plays a critical role in supporting AstraZeneca’s R&D presence in Beijing, one of the company’s six strategic global sites. As a key site representative for R&D China, this role
Major Responsibilities Leadership of group work and building the team spirit, including developing team style and behaviour Ensuring adequate resources for the studies assigned Ensure that the workload of the team(s) or direct reports is adequate
Major Responsibilities Leadership of group work and building the team spirit, including developing team style and behaviour Ensuring adequate resources for the studies assigned Ensure that the workload of the team(s) or direct reports is adequate
Serve as SDTL Responsible for planning and leading the delivery of all components of a clinical study to time, cost, and quality from Study Specifications (SS) through study closeout activities and Clinical Study Report (CSR). Form
Serve as SDTL Responsible for planning and leading the delivery of all components of a clinical study to time, cost, and quality from Study Specifications (SS) through study closeout activities and Clinical Study Report (CSR). Form
Typical Accountabilities: Takes medical responsibilities to ensures successful conduct and integrity of all in-scope clinical studies Work as China study physician in China-join global studies, PK studies or country-specific clinical initiatives under the supervision from program/study
Overview This position is located at AGs Beijing office. Please apply to another open job posting if you would like to be considered for a position outside of Beijing. Given the volume of applications we receive,
About the Beijing AI Center The Beijing AI Center is a new strategic investment by AstraZeneca to accelerate drug discovery through AI. The center brings together AI researchers, computational scientists, and platform engineers to apply foundation