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- To lead and be accountable for end-to-end delivery of the assigned Therapeutic Area (TA) portfolio within RCO Japan, by directing both the Clinical Trial Management (CTM) and Clinical Research Associate (CRA)/Site Management line functions as a single, integrated operating mode
• 分析所负责辖区市场情况，明确市场潜力、重点客户及对应品牌策略，制定相应的业务计划，最大程度地开发辖区内的潜在市场，并确保业务目标的达成； • 用合规的方式执行相应的业务计划并对实施进行管理与评估，确保辖区内业务活动的执行符合公司政策和流程的要求； • 及时洞察辖区市场状态并向上级主管反馈竞争状况等市场信息，依据市场现状适当调整业务计划，并提出反馈建议； • 执行区域的准入计划，确保公司产品在医
- Develop and integrate AI-enabled features within the Veeva CRM/Vault CRM ecosystem — including LLM-based solutions using industry standard models like Claude accessed directly or via AWS Bedrock under the direction of the engineering manager. - Support the implementation of AI/
When you join BMS, you are joining a high-achieving team united by a common mission. The Informatics and Predictive Sciences (IPS) mission is to Pioneer, Partner and Predict to drive transformative insights for patient benefit. IPS conducts applied computational research in area
RayzeBio is seeking an Associate Director, In‑Vivo Pharmacology to provide scientific and operational leadership across oncology programs with a focus on radiopharmaceutical therapeutics (RPTs). This role provides functional leadership to senior scientists to design and execute h
Job Description Summary: The Senior Manager, Corporate Affairs, will lead the design and execution of strategic communications and corporate engagement initiatives for the BMS based out of Hyderabad, supporting the organization’s reputation, employee engagement, and stakeholder
The Receptionist serves as the first point of contact for staff, vendors and external guests, providing a professional and welcoming presence at the front desk of a busy biopharmaceutical office. This role is responsible for managing incoming communications, coordinating visitor
The Senior Director, Global Clinical Physician is the primary source of medical accountability and oversight for one or more Oncology clinical trials within the Drug Development organization. The incumbent will be accountable, alongside the Clinical Development Program Lead, for
The Senior Bioprocess Associate uses current Good Manufacturing Practices (cGMPs) in the execution of commercial manufacturing processes for the manufacture of therapeutic proteins used in medicines that are revolutionizing the treatment of serious disease. - Works on routine ma
The Director, Quality Compliance at the BMS Summit West Cell Therapy (CAR T) Manufacturing Facility in Summit, NJ is responsible for the development, implementation, enhancement, and continuous improvement of site Compliance. The role will work collaboratively across BMS to ensur
This position will be responsible for conducting research, experiments, and analysis in the field of radiochemistry. This role involves radiolabeling of diagnostic and therapeutic radioisotopes of peptides, small molecules, and/or antibodies as well as quality testing for in vitr
Senior individual-contributor role on the Architecture and Components team; works alongside a multidisciplinary group (UI, UX, AI Engineering, Full Stack, Architecture) within a globally distributed organization. This role does not manage people. As BMS Product Development & Sup
Define and lead the Precision Medicine strategy for China in partnership with global asset teams, China development teams, translational medicine, regulatory, clinical operations, medical, and commercial stakeholders. Develop and execute China-focused Precision Medicine strategi
Summary: The Cryogenic Process Associate/Specialist assists in the execution of drug substance freezing, drug substance and QC sample shipments according to established work instructions and production records for the manufacture of therapeutic proteins in accordance with current
The Senior Director, Global Medical Neuroscience, Psychiatry, Mood Disorders will serve as a senior medical and scientific leader responsible for shaping and driving the global medical strategy for BMS's Mood Disorders portfolio. This role will provide strategic direction and lea
The Clinical Trial Manager (CTM) is accountable for end-to-end study operational oversight and delivery at country level, ensuring adherence to timelines, budget and quality standards. Acts as the primary point of contact at a country level for both internal and external stakehol
The Director of Medical Evidence Generation in Medical Affairs will lead the strategic development and execution of a robust evidence generation plan for an important asset within the Oncology portfolio, focused primarily in gastrointestinal (GI) and genitourinary (GU) cancers, i
When you join BMS, you are joining a high-achieving team united by a common mission. The Informatics and Predictive Sciences (IPS) mission is to Pioneer, Partner and Predict to drive transformative insights for patient benefit. IPS conducts applied computational research in area
Shape the Future of AI-Driven Pharmaceutical Product Development (PD) In our pharmaceutical product development team at Bristol Myers Squibb in Hyderabad, we are focusing on building advanced and emerging GenAI, data science and engineering, and modelling approaches addressing c
- 深入分析辖区市场环境、竞争格局，结合品牌策略识别区域业务机会，合理配置资源制定业务发展计划； - 带领团队合规实施业务计划，与客户进行有效互动，最大程度地开发辖区内的潜在市场确保团队绩效目标达成； - 定期开展业务复盘与分析，建立业务预测机制评估业务风险并制定应对措施及时调整，确保区域目标达成； - 熟悉辖区医保、商保、患者支持项目决策流程及关键利益相关方，推动医院准入及产品覆盖； - 深入了解关键