POSITION SUMMARY: The primary responsibility of the CMC Regulatory Affairs Associate Director is to provide CMC RA supports for the submissions in China with a focus on chemical products. He/she will also support chemical product CMC
A Site Manager II (SM II) serves as the primary contact point between the Sponsor and the Investigational Site. A Site Manager II is assigned to trial sites to ensure inspection readiness through compliance with the
The Associate Director, Product Stewardship ASPAC is responsible for executing on all Product Stewardship requirements for the ASPAC region of the J&J MedTech businesses. , The Associate Director is responsible for ensuring that the ASPAC MedTech
Position Summary: (Briefly state the objectives of this position) A Site Manager II (SM II) serves as the primary contact point between the Sponsor and the Investigational Site. A Site Manager II is assigned to trial
Position Summary: (Briefly state the objectives of this position) The Local Trial Manager II (LTM II) is responsible for local management of a clinical trial (or Medical Affairs data generation activity) in a country or countries.
Main responsibilities The Senior Privacy manager of R&D, Johnson & Johnson Innovative Medicine CHINA is responsible for implementing and monitoring the privacy compliance program for all R&D activities in China, identifying privacy risks and developing policies and procedures,
SUMMARY: Support Health Care Compliance (HCC) director to implement HCC program to ensure business practices and activities in compliance with related Johnson & Johnson (J&J) internal guidelines, local laws and regulations and anti corruption laws including the U.S.
主要职责: 1. 高效执行公司市场部的策略,达成及超越公司制定的业务目标; 2. 有效地将目标客户进行分级管理,合理安排拜访频率,确保在拜访执行过程中准确传递产品信息; 3. 依照公司合规要求,独立组织学术幻灯演讲以及支持区域内的会议 / 活动推广工作; 4. 实时维护工作相关数据,以便准确且及时地反应市场状态; 5. 协助主管完成招标和医保事务及职责范围内部门安排的其他工作任务; 任职要求: 1. 统招本科及以上学历,并获得学士及以上学位,专业不限(特殊产品需要医药背景); 2. 2 年及以上医药行业相关工作经验; 3. 试用期内通过中国外商投资企业协会药品研制和开发行业委员会 ( RDPAC ) 举办的 MRC 测试取得不低于 80 分的成绩,以及按照公司要求完成入职培训,合规培训及考核并达到相关要求(该等条件和要求属于员工应满足的录用条件,如未能按照公司要求完成相关测试,培训并满足考核,将视为试用期内不符合录用条件。) 4. 较强的业务敏锐度, 解决问题能力及客户管理能力; 5. 优秀的学习与运用的能力,沟通与说服能力,项目管理能力及业务规划与执行能力; 6. 不畏艰难,具有坚持不懈追求成功与卓越的挑战精神以及团队合作精神;
• Be accountable of business partner for ONCO BU, especially in business analysis and project management under manager supervision. • Work collaboratively with marketing & sales team and relative stakeholders to ensure a smooth design and
1. 高效执行公司市场部的策略,达成及超越公司制定的业务目标; 2. 有效地将目标客户进行分级管理,合理安排拜访频率,确保在拜访执行过程中准确传递产品信息; 3. 依照公司合规要求,独立组织学术幻灯演讲以及支持区域内的会议 / 活动推广工作; 4. 实时维护工作相关数据,以便准确且及时地反应市场状态; 5. 协助主管完成招标和医保事务及职责范围内部门安排的其他工作任务;1. 医药相关专业,统招本科及以上学历,并获得学士及以上学位; 2. 2 年及以上医药行业相关工作经验; 3. 较强的业务敏锐度, 解决问题能力及客户管理能力; 4. 优秀的学习与运用的能力,沟通与说服能力,项目管理能力及业务规划与执行能力; 5. 不畏艰难,具有坚持不懈追求成功与卓越的挑战精神以及团队合作精神; 6. 熟练应用 Office 等办公操作软件; 7. 在中国外商投资企业协会药品研制和开发行业委员会 ( RDPAC ) 举办的 MRC 测试取得不低于 80
支持医学卓越团队的项目运营及日常工作,例如: 1. 协助部门做好相关数据收集,整理,分析和报告准备; 2. 支持部门培训项目,文化活动及其他团队活动的策划,组织及现场执行等; 3. 幻灯及其他内容美化,海报设计及简单视频剪辑等; 4. 其他日常工作。1. 本科以上学历,专业不限,医学,药学,生物学,公共卫生等生物医药相关专业优先,具备医药行业特别是 MNC 实习经验者优先; 2. 具备良好的英语读写能力; 3. 熟练使用相关办公软件( Word, Excel, PPT, 视频剪辑等); 4. 良好的团队合作,人际沟通及解决问题能力; 5. 实习时间要求:至少 3 个月,每周至少 3 天...