Chief Medical Officer (CMO)

About VyBio VyBio focuses on the global innovative pharmaceutical sector, building an internationally competitive platform for pharmaceutical R&D and commercialization. We deepen our layout in core therapeutic areas, drive the translational application of cutting-edge pharmaceutical research outcomes, and deliver high-quality medical solutions for patients worldwide. We sincerely invite outstanding medical leaders with a multinational pharmaceutical perspective and top-tier professional capabilities to join us and co-create a new blueprint for pharmaceutical innovation. Work Location: Hangzhou, China, Job Responsibilities · Lead the implementation of global clinical R&D strategies, oversee end-to-end medical management of innovative drugs throughout their life cycles, and steer the direction, progress and quality of clinical development. · Be responsible for the design and optimization of clinical trial protocols, organize multicenter clinical trials, coordinate internal and external resources, and ensure the efficient advancement of trials in compliance with FDA and international regulatory requirements. · Establish a medical risk management system, analyze and evaluate clinical safety data and submit required reports, formulate risk control strategies, and safeguard the safety of study subjects. · Build and lead the medical team, define the organizational structure and job responsibilities, cultivate core talents, and develop a high-performance, professional R&D team. · Participate in product pipeline planning and project initiation evaluation, and provide professional support for the differentiated positioning of products and exploration of their clinical value. · Cultivate relationships with world-class clinical experts, academic institutions and regulatory authorities, participate in industry exchanges, and enhance the company’s influence in the sector. · Collaborate with multiple departments to provide professional guidance for post-launch medical promotion, indication expansion and real-world evidence (RWE) research of products. Job Requirements · Doctoral degree in clinical medicine or related disciplines (priority given to Internal Medicine, Oncology and other relevant specialties), with a solid medical theoretical foundation and clinical practice experience. · More than 5 years of experience in clinical R&D or medical management at multinational pharmaceutical corporations (MNCs), familiar with the entire clinical development process of innovative drugs; candidates with a proven track record of successfully advancing drugs from clinical development to market approval are preferred. · Proficient in FDA and international pharmaceutical regulatory laws, regulations and Good Clinical Practice (GCP), with extensive experience in regulatory communications and the ability to effectively respond to regulatory inspections and inquiries. · Possess outstanding strategic thinking, project management capabilities and risk anticipation ability, and be able to formulate scientific and rational clinical R&D strategies and drive their implementation in complex environments. · Demonstrate excellent leadership and team management skills, excel at building and empowering teams, have strong cross-departmental and cross-cultural collaboration capabilities, and can efficiently coordinate global resources. · English as a working language, with fluent listening, speaking, reading and writing skills; able to proficiently compose English clinical reports and participate in international academic exchanges and negotiations. · Able to adapt to a global work rhythm and meet international travel requirements. What We Offer A highly competitive compensation and benefits package, a global career development platform, equity incentives for core team members, a comprehensive training system with tailored career planning, and opportunities to work with top talents in the pharmaceutical industry, empowering you to achieve a leap in professional value. Application Method Please send your personal resume in both Chinese and English to: [email protected]. Mark the email subject as: Name - Applied Position - Sourced from LinkedIn. We will conduct resume screening as soon as possible upon receipt, and qualified candidates will be contacted for an interview. About VyBio VyBio focuses on the global innovative pharmaceutical sector, building an internationally competitive platform for pharmaceutical R&D and commercialization. We deepen our layout in core therapeutic areas, drive the translational application of cutting-edge pharmaceutical research outcomes, and deliver high-quality medical solutions for patients worldwide. We sincerely invite outstanding medical leaders with a multinational pharmaceutical perspective and top-tier professional capabilities to join us and co-create a new blueprint for pharmaceutical innovation. 关于扬厉医药​ 扬厉医药聚焦全球创新医药领域，打造具有国际竞争力的医药研发与商业化平台，深耕核心治疗领域，推动前沿药物成果转化，为全球患者提供更优质的医疗解决方案。我们诚邀具备跨国药企视野与顶尖专业能力的医疗领军人才加入，共筑医药创新新蓝图。​ 混合办公地点：中国浙江杭州 岗位职责​ •主导全球临床研发战略落地，统筹创新药全生命周期医学管理，把控临床开发方向、进度与质量。​ •负责临床试验方案设计优化，组织多中心试验，协调内外部资源，确保符合FDA及国际法规高效推进。​ •搭建医学风险管理体系，分析评估临床安全性数据并上报，制定风险控制策略，保障受试者安全。​ •搭建并领导医学团队，明确架构职责，培养核心人才，打造高绩效专业化研发团队。​ •参与产品管线布局与项目立项评估，为产品差异化定位、临床价值挖掘提供专业支撑。​ •维护全球顶尖临床专家、学术机构及监管部门关系，参与行业交流，提升公司影响力。​ •协同多部门，为产品上市后医学推广、适应症拓展及真实世界研究提供专业指导。​ 任职要求​ •博士学历，临床医学相关专业（内科学、肿瘤学等方向优先），具备扎实的医学理论基础与临床实践经验。​ •拥有5年以上跨国药企（MNC）临床研发或医学管理工作经验，熟悉创新药临床开发全流程，有成功推动药物从临床到上市的项目经验者优先。​ •精通FDA及国际医药监管法规与临床研究规范（GCP），具备丰富的监管沟通经验，能够高效应对监管核查与问询。​ •具备卓越的战略思维、项目管理能力与风险预判能力，能够在复杂环境中制定科学合理的临床研发策略并推动落地。​ •拥有出色的领导力与团队管理能力，善于搭建和赋能团队，具备跨部门、跨文化协同合作能力，能够有效协调全球资源。​ •英语为工作语言，具备流利的听说读写能力，能够熟练撰写英文临床报告、参与国际学术交流与谈判。​ •能够适应全球化工作节奏与出差需求。​ 我们提供​ 极具竞争力的薪酬福利体系、全球化职业发展平台、核心团队股权激励、完善的培训体系与个性化职业规划，以及与行业顶尖人才共事的机会，助力你实现职业价值跃升。​ 申请方式​ 请将个人中英文简历发送至邮箱：[email protected]，邮件主题注明“姓名-应聘岗位-来源领英”，我们将在收到简历后尽快进行筛选，合则约见。