Beijing, Beijing, China · On-site
Typical Accountabilities: - In partnership with AZ enablement team, other AZ clinical experts and external service providers, the GSAM provides oversight to ensure study delivery. - Leads/contributes to the preparation o…
Skills: Clinical Study Oversight, CRO Management, Project Management, ICH/GCP Guidelines, Budget Management
Beijing, Beijing, China · On-site
By clicking the “Apply” button, I understand that my employment application process with Takeda will commence and that the information I provide in my application will be processed in line with Takeda’s Privacy Notice an…
Skills: Drug Registration, Regulatory Affairs, Project Leadership, Technical Leadership, Compliance Management
Beijing, Beijing, China · On-site
Typical Accountabilities: - In partnership with AZ enablement team, other AZ clinical experts and external service providers, the GSAM provides oversight to ensure study delivery. - Leads/contributes to the preparation o…
Skills: Clinical Study Oversight, CRO Management, Project Management, ICH/GCP Guidelines, Budget Management
Beijing, Beijing, China · On-site
By clicking the “Apply” button, I understand that my employment application process with Takeda will commence and that the information I provide in my application will be processed in line with Takeda’s Privacy Notice an…
Skills: Regulatory Affairs, Product Registration, Drug Administration Laws, Technical Leadership, Stakeholder Management
Beijing, Beijing, China · On-site
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). Main…
Skills: eTMF Management, ICH/GCP Guidelines, Clinical Trial Transparency, Regulatory Documentation, Budget Tracking
Beijing, Beijing, China · On-site
Job Description 职位描述： 在指定的区域内积极开展公司产品的介绍和推广，与医疗机构建立并维持良好的合作交流关系，确保公司下达的各项推广目标的达成，同时确保公司产品的市场占有率和增长率。 工作职责： 区域目标 在指定的区域内, 达到指定产品的目标，市场占有率和增长率,并有效地利用资源和控制费用按照公司规定的医疗机构覆盖和拜访频率，制定相应医疗机构的拜访计划并实施运用适当的推广技巧和有效地利用产品资料,向医疗机构提供医疗咨讯…
Skills: Account Management, Adaptability, B2B Sales, Clinical Experience, Customer-Focused
Beijing, Beijing, China · Hybrid
Clinical Research Associate II， China ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. As a values-driven organisat…
Skills: Clinical Trial Monitoring, Protocol Compliance, Data Integrity, Patient Safety, ICH-GCP Guidelines
Beijing, Beijing, China · On-site
工作摘要/目的Job Summary / Purpose 根据公司业务计划，进行日常产品学术推广及产品操作规范培训等活动，以完成个人业务目标。 主要职责/责任Essential Duties / Responsibilities 根据公司业务计划，进行日常业务活动，以完成个人业务目标； 开发与维护专业客户，保持长期良好的合作关系，并为客户提供专业的产品知识与相关服务； 独立组织所负责区域内/目标医院内各类学术活动及专业的学习研讨会； 收…
Skills: Communication And Coordination, Regional Management, Problem Solving, Data Analysis, Visitation Techniques
Beijing, Beijing, China · Hybrid
Job TitleGovernment Affairs Intern Job Description Your role: The Government Affairs team needs strengthened policy research, government liaison and internal coordination support. An intern is required to ease daily work…
Skills: Policy Research, Government Liaison, Internal Coordination, Data Sorting, Document Organizing
Beijing, Beijing, China · Remote OK
At Medtronic you can begin a life-long career of exploration and innovation, while helping champion healthcare access and equity for all. You’ll lead with purpose, breaking down barriers to innovation in a more connected…
Skills: Technical Sales, Account Management, Market Research, Relationship Building, Contract Negotiation
Beijing, Beijing, China · On-site
职衔：特药事业部-医学信息沟通代表 地点：北京 关于工作 作为我们特药事业部的医学信息沟通代表，您将加入团队，为有免疫挑战、罕见病、癌症和神经系统疾病的患者提供转化护理。在特药事业部中，您将帮助提供突破性的治疗，为有最高未满足需求的患者带来希望 关于赛诺菲： 我们是一家以研发为驱动、以AI为动力的生物制药公司，致力于改善人们的生活并实现令人信服的增长。我们对免疫系统的深入理解以及创新的产品管线使我们能够发明药物和疫苗，为全球数百万人提供…
Skills: Academic Promotion, Customer Management, Execution Ability, Resilience, Learning Agility
Beijing, Beijing, China · On-site
Job Description 职位描述： 在指定的区域内积极开展公司产品的介绍和推广，与医疗机构建立并维持良好的合作交流关系，确保公司下达的各项推广目标的达成，同时确保公司产品的市场占有率和增长率。 工作职责： 区域目标 在指定的区域内, 达到指定产品的目标，市场占有率和增长率,并有效地利用资源和控制费用按照公司规定的医疗机构覆盖和拜访频率，制定相应医疗机构的拜访计划并实施运用适当的推广技巧和有效地利用产品资料,向医疗机构提供医疗咨讯…
Skills: Account Management, Customer Relationship Management (CRM), Oncology Sales, Market Analysis, Lead Generation
Beijing, Beijing, China · On-site
与我们携手施展你的超能力！ 探索未知、打破壁垒、勇于发现，你准备好了吗？你有宏图大志正待实现，我们同样雄心勃勃。我们遍布全球的员工热爱科技创新，以医药健康、生命科学和电子科技领域的解决方案，切实改善人类生活。我们怀揣远大梦想，热忱关爱员工、客户、患者和人类居住的这颗星球。因此我们一直在寻找永葆好奇心的你，与我们一路同行、敢想敢做，把不可能变为可能！ 在医药健康领域，我们团结一致，齐心为病患，帮助孕育、改善和延长生命。这是我们的目标，也是…
Skills: Market Analysis, Business Planning, Sales Execution, Relationship Management, Presentation Skills
Beijing, Beijing, China · On-site
公司介绍 艾伯维的使命是发现和提供创新药物，解决复杂且棘手的疾病难题和未来的医学挑战。我们不懈努力，凭借在多个关键治疗领域的科研创新为人们的生活带来深远影响，包括免疫学、肿瘤学、神经科学，以及艾尔建美学产品组合中的产品和服务。有关艾伯维的更多信息，请访问网站 https://www.abbvie.com。在领英、Facebook、Instagram、X 和 YouTube 上关注AbbVie。 职位描述 高级专业医药代表（免疫 ） 负责…
Skills: Sales, Customer Relationship Management, Market Analysis, Communication, Medical Knowledge
Beijing, Beijing, China · Hybrid
Clinical Research Associate, Beijing, office base ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. As a values-driv…
Skills: Clinical Trial Monitoring, GCP Standards, Site Management, Data Integrity, Stakeholder Management
Beijing, Beijing, China · On-site
职衔：特药事业部-医学信息沟通代表 地点：北京 关于工作 作为我们特药事业部的医学信息沟通代表，您将加入团队，为有免疫挑战、罕见病、癌症和神经系统疾病的患者提供转化护理。在特药事业部中，您将帮助提供突破性的治疗，为有最高未满足需求的患者带来希望 关于赛诺菲： 我们是一家以研发为驱动、以AI为动力的生物制药公司，致力于改善人们的生活并实现令人信服的增长。我们对免疫系统的深入理解以及创新的产品管线使我们能够发明药物和疫苗，为全球数百万人提供…
Skills: Academic Promotion, Customer Management, Execution Ability, Resilience, Learning Agility
Beijing, Beijing, China · On-site
7月第六届第二批管培生招聘 Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates. To learn more about acceptable and prohibited use…
Beijing, Beijing, China · Remote OK
Job Overview: The Clinical Trial Manager I has ownership in the clinical delivery and operational oversight of clinical research trials. This role collaborates with project managers and other functional leads to deliver …
Skills: Clinical Trial Management, Project Management, Risk Management, Budget Forecasting, Site Activation
Beijing, Beijing, China · On-site
Job Description This role is primarily accountable for the end-to-end performance and project management for assigned protocols in a country in compliance with ICH/GCP and country regulations, company policies and proced…
Skills: Adverse Event Report, Clinical Research Methods, Clinical Site Management, Clinical Study Management, Clinical Trial Planning
Beijing, Beijing, China · On-site
Contract type: Fixed Term Bracco is an international Group active in the healthcare sector and a leader in diagnostic imaging. The Group’s main products are contrast agents sold in over 100 countries, both directly and i…
Skills: Account Management, Client Relationship Management, Diagnostic Imaging, Medical Information, Sales Revenue Driving
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The Global Study Associate Manager provides oversight for study delivery by managing external service providers and collaborating with internal functions. Key duties include preparing study documents, managing budgets, and ensuring compliance with ICH/GCP guidelines to keep studies inspection-ready.
Candidates should hold a university degree in medical or biological sciences and have at least 3 years of experience in the pharmaceutical industry. Proficiency in clinical development processes, ICH/GCP guidelines, and project management is required.
- In partnership with AZ enablement team, other AZ clinical experts and external service providers, the GSAM provides oversight to ensure study delivery.
- Leads/contributes to the preparation of delegated study documents (e.g. Informed Consent Form, Master Clinical Study Agreement etc), and external service provider related documents (specifications, study specific procedures, descriptions, presentations etc.)
- Maintains and facilitates interactions with internal functions including but not limited to Enablement, Data Management, Procurement, Regulatory, Patient Safety and Quality Assurance, and external functions including the CROs and other external service providers to ensure an efficient study delivery to time, costs and quality objectives
- Contributes to the planning and conduct of internal and external meetings (e.g. Investigators’/Monitors’ meeting)
- Ensures the supply of Investigational product and study materials by liaising with Clinical Supply Chain or external service providers as appropriate
- Proactively contributes to risk and issue identification, development of mitigation and/or action plans for identified risks and issues
- Ensures that all study documents in scope of GSAM’s responsibilities are complete and verified for quality in Trial Master File
- Supports Global Study Leader (GSL) with budget management, such as external service provider invoice reconciliation
- Adheres to global clinical processes, procedural documents, applicable Quality & Compliance manual documents and international guidelines such as ICH/GCP to ensure study is inspection ready at all times
- Supports Global Study Leaders (GSL) in project management as per agreed delegation
- For outsourced studies, supports Global Study Leader (GSL) in management of the CRO
- Project Manager to ensure study delivery according to agreed timelines, budget and quality standards,
o while ensuring that the appropriate level of oversight of the CRO is maintained and documented
o throughout the lifecycle of the study, in accordance with relevant AZ SOPs and
o guidelines (e.g. description of services and transfer of obligations)
- Take on assignments on non-drug project work in process improvements and/or leading improvement projects as discussed and agreed upon with their manager
- University degree (or equivalent), preferably in medical or biological sciences or discipline associated with clinical research.
- Relevant experience from within the pharmaceutical industry or similar organization or academic experience, preferably of at least 3 years.
- Knowledge of clinical development / drug development process in various phases of development and therapy areas
- Excellent knowledge of international guidelines ICH/GCP
- Excellent communication and relationship building skills, including external service provider management skills
- Good project management skills
- Demonstrated ability to collaborate as well as work independently
- Demonstrated leadership skills
- Computer proficiency, advanced computer skills in day-to-day tasks
- Experience in all phases of a clinical study lifecycle
- Basic knowledge of GXP outside of GCP (i.e GMP/GLP)
- Excellent verbal and written communication in English
AstraZeneca embraces diversity and equality of opportunity. We are committed to building an inclusive and diverse team representing all backgrounds, with as wide a range of perspectives as possible, and harnessing industry-leading skills. We believe that the more inclusive we are, the better our work will be. We welcome and consider applications to join our team from all qualified candidates, regardless of their characteristics. We comply with all applicable laws and regulations on non-discrimination in employment (and recruitment), as well as work authorization and employment eligibility verification requirements.
We're transforming the future of healthcare by unlocking the power of what science can do for people, society and the planet. For more information, visit www.astrazeneca.com. Community Guidelines: bit.ly/2MgAcio
Offices: 1 Francis Crick Avenue, Cambridge Biomedical Campus, Cambridge, Cambridgeshire CB2 0AA, GB · Astraallen, Sodertalje, Stockholm County 152 57, SE
There are currently 221 open healthcare positions in Beijing, China listed on Clera. New openings are added daily as companies post roles.
Companies currently hiring include IQVIA, Sanofi, ICON plc, Johnson & Johnson Innovative Medicine, MSD, among others. Browse the listings above to see every active employer.
Yes — 46 of the 221 open healthcare positions offer remote or hybrid work (10 remote, 36 hybrid).
Each listing links directly to the employer's application page. Apply early — fresh listings get the most recruiter attention in the first two weeks.
