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R&D VP, 该职位将作为研发负责人,直接汇报给公司CEO,带领研发团队,统筹管理研发各个模块,包含如芯片、材料、试剂体系开发、信号电路、信号处理算法等各模块;控制项目成本,协助攻克产品技术难点,实现工程化样机落地,最终完成产品商业化
全面负责公司的产品市场推广、销售、渠道管理事务,统筹制定公司营销战略、商务运营管理和市场营销团队建设等
注册总监,直接汇报给公司CEO,带领注册团队完成国内国际注册。
为细胞治疗和抗体等相关领域的早期发现和临床前研发工作制定中长期战略目标,结合行业趋势和内部优势,开发有潜力的产品,并推动其商业化进程;
Perform site selection (If applicable )), initiation, monitoring and close out visits in accordance with contractedscope of work and good clinical practice. P erform study start up activities, including site EC submission,contract negotiation, etc. If applicable, Clinical Research Associates may be accountable for development ofproject subject recruitment plan on a per site basis.
Report to the Board, comprehensively preside over the daily operation and management of the company. Achieve the company's listing goal.
As RA Head, responsible for full RA job from strategy to project operation.
Managing complete drug variations
组织和开展医学撰写工作,在产品研发重要里程碑节点汇总、整理、提交注册申报资料;
Head of Translational R&D Vaccine, located in Shanghai, leading both in vivo animal study and in vitro assay development groups, working on the vaccine candidates' evaluation and down selection utilizing in vivo and in vitro studies, across company expanding portfolio of early and late-stage vaccine candidates.
As the Chief of Staff of the company, this role will be closely working with the CEO and proactively managing and contributing to the meet company's strategic, and growth initiatives i.e R&D strategies, commercialisation strategies, critical project management;
This role is designed to acquire and synthesise relevant information from varies sources and present actionable insights to support the initiation and continuous development of internal portfolio of products.
This is a newly created Alliance Management role for a high potential biopharma. As the Director/Senior Director, this role will be working with the top-notch talents in business development and alliance management professional across the global and playing a critical role in managing a portfolio of alliances, assisting the pipeline development and bridging the internal and external stakeholders to ensure the on-going projects are well managed.
根据新产品的研发计划,编制产品技术要求及风险文件;
负责公司小分子创新药研发项目的管理
适合2-3年药物警戒经验、对外资药企感兴趣的人选
中国区RA HEAD负责整个国内的注册策略制定,团队的搭建,以及管线产品的注册。
负责包括上市前及后的医学管理,临床运营,临床质量, PV以及biometrics的管理;
搭建,组织小核酸团队和平台,领导团队推进小核酸项目并完成相应的节点