求职者
浏览我们的职位并开启您的下一步申请
雇主
只需点击几下,即可找到合适的候选人。
关于我们
Michael Page通过创造挖掘潜能,让您绽放自我,成就精彩人生
联系我们
如果您有任何问题,我们很乐意为您提供帮助。
We are looking for an experienced discovery professional combining scientific depth, innovative thinking and team leadership to build drug discovery capabilities from the ground up, advance programs from scientific concepts to PCC/IND, and explore the application of AI and emerging modalities in innovative drug discovery.
Join a rapidly expanding biotech as CSO, advanced scientific innovation from target identification through preclinical development while building a differentiated pipeline in oncology and immunology. We are looking for an industry-proven scientific executive with strong portfolio evaluation and drug discovery experience.
Join an innovative biotech to lead early clinical development across a growing Immunology & Inflammation pipeline, with responsibility spanning Phase 1/2 strategy, study design, medical oversight and clinical decision-making.
The Global Director, Quality Assurance & Regulatory Affairs will lead the company's global QARA function, overseeing quality systems, regulatory compliance, audits, supplier quality, and market access activities across international markets. This role will manage a team of QA and RA professionals while collaborating with cross-functional stakeholders, external regulatory bodies, notified bodies, distributors, and regional regulatory partners worldwide.
Play a key role in the design and optimization of therapeutic peptides, peptide-drug conjugates (PDCs), and macrocyclic molecules. Work closely with our US-based scientific leadership and cross-functional discovery teams to translate innovative ideas into high-quality intellectual property and pipeline assets.
负责从靶点验证、药效评价、PD Biomarker开发到IND申报支持的全流程药理研究,兼顾团队指导与实验方案设计工作。
负责搭建和领导多肽药物分析研发平台,统筹分析方法开发、技术转移、注册申报及商业化支持等全生命周期分析工作。带领高水平团队解决复杂多肽药物分析技术挑战,推动创新项目高质量交付并支撑公司全球化发展。
We are looking for an experienced CMO to lead the medical strategy and clinical development of our stem cell and regenerative medicine portfolio.
作为集团首席科学官,负责统筹多个研发平台及研究院的科学战略、技术决策与创新协同,通过科学领导力推动组织共识形成、资源优化配置及创新研发体系持续升级。
This role is responsible for developing and implementing China-focused early clinical development strategies to generate high-quality, decision-driving data for global programs across genetic neurological, renal, pulmonary, and other rare genetic diseases.
You will lead translational research and early clinical development strategies, bridging discovery science with clinical application. The position combines scientific leadership, operational oversight, and regulatory engagement to accelerate innovative therapies toward commercialization.
As RAQA Manager, you will be responsible for driving the regulatory and quality strategy for China registration of a Class II active medical device. You will collaborate closely with cross-functional teams and external stakeholders to ensure timely and compliant market entry.
The VP of Corporate Strategic Investment is responsible for identifying, executing, and integrating inorganic growth, revenue-generating technology platform M&A deals that accelerate the company's commercial and operational capabilities.
In partnership with the CEO, the position holder will lead the company's science and research strategy and implementation. The person will take leadership role in shaping the scientific strategy and bringing new product into the company to build strong product pipeline. He/she will identify potential leads, formulate transaction model, lead business negotiation, and manage the execution of the transactions
In partnership with the CEO, the position holder will lead the company's business development strategy and implementation. The person will take leadership role in shaping the portfolio strategy with focus on out-licensing and partnership opportunities. The candidate will identify potential leads, formulate transaction model, lead business negotiation, and manage the execution of the transactions.
The Medical Director China will be responsible for incorporating and executing the local medical plan developed from the Global Medical and Marketing Strategical Plan incorporating local market and medical insights. This person will be accountable for Medical Governance and the medical ethical standards within the Country Organisation and takes full responsibility for the medical management in China - drives and leads all medical activities.
Provide scientific expertise in local registration clinical trials. and license-in OTC products.Provide medical contributions in developing and implementing marketing strategy.
负责制定并领导公司创新药管线的临床开发战略,推动项目从IND申报、早期临床研究到关键开发阶段,并带领团队实现全球临床开发目标。
创建职位提醒,一旦有新的Healthcare 生命科学相关职位发布,您将第一时间通过电子邮件收到通知。
提交您的简历并完成注册。如果有适合您的职位机会,我们将主动与您联系。