דרושים ב-Msd ב-China, Lianhu District

The Safety Data Lead I is responsible for the analysis and interpretation of adverse experience (AE) reports of varying complexity, in compliance with regulatory requirements and internal processes. Working under...

深入洞察区域疫苗市场动态、竞争对手情况及客户等信息，制定区域策略和目标，带领团队协同合作伙伴智飞完成目标，实现业务的可持续增长。. 与智飞管理层就中长期业务目标达成一致，建立互信和定期沟通机制，推动关键目标的执行落地. 协助智飞总监搭建高绩效团队，提升团队能力以支持共同目标的执行落地. 管理区域内有影响力的疾控领域专家，发展全国KOL及讲者，建立长期合作关系. 助力疫苗生态体系的建立和完善，协同智飞完善标准化的疫苗接种服务流程，推动建立线上线下预约和科普体系. 协同跨部门推进PIP/CIP等重大项目落地，推动校园及企业大客户接种，私立医院等创新渠道建设. 搭建完善的团队管理体系，通过赋能，授权和委责来发动下一层的管理者来实现目标. 重视团队培养，针对团队特性分层次的对团队进行培养和发展，能够对下属进行领导力的辅导和培养。. 制定有效的团队激励，营造积极的团队氛围，打造良性的团队文化. 确保工作过程严格遵守公司的各项SOP和财务制度。. 保证团队和合作伙伴的行为符合公司合规要求。....

Develops strong site relationships and ensures continuity of site relationships through all phases of the trial. Performs clinical study sitemanagement/monitoringactivities in compliance with ICH-GCP, Sponsor SOPs, Local Laws & Regulations,...

A. Position Objective. We are looking for a highly motivated individual with expertise in drug design, synthesis, as well as small molecule drug development and evaluation. The overall role is...

Project Manager Protocol (Hybrid)Working independently, the Protocol Clinical Supplies Project Manager (Protocol CSPM) designs strategic and operational plans for all activities associated with clinical supplies for their assigned studies, which...

The Safety Data Lead I is responsible for the analysis and interpretation of adverse experience (AE) reports of varying complexity, in compliance with regulatory requirements and internal processes. Working under...

Performing analysis, interpretation, and data entry of adverse event reports from a wide range of sources and therapeutic areas, demonstrating increasing proficiency in clinical knowledge, GPVCM processes and regulatory guidelines....