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更新:2024-04-14
医学总监
7-9万
成都双流县  | 3-5年  | 硕士  | 社招
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五险一金
Position: Medical Director
Report to: CMO 
Location: Chengdu or Shanghai

Responsibility and Key Activities 
Accountable for the generation of development strategy study design and Clinical Development Plan via closely communication with KOLs/investigator
Accountable for all medical related documents preparation at IND and NDA phase
Working as drug development expert to lead and/or participate relevant medical activity. 
Ensures “best practice” in all activities and effective implementation and optimization of process improvements. 
Keeping vigilant on R&D advancement, acknowledging the guideline, academic progress and trends of the related therapeutic area, reading related reference/documents, attending academic conference. 
Accountable for the execution of all data-generating activities (studies) is compliant to ICH/GCP standards, Company SOPs, operating guidelines, legal and financial standards and practices. 
Develops a highly motivated team through effective leadership, coaching and people management, ensuring an objective and performance-led management culture. 
Accountable for resource management, performance management and career development of medical team. 

Education 
Clinical medical degree is a must.
Master’s degree or Ph.D in Medicine or equivalent degree. 

Experience and Knowledge 
M.D. with medical practice experience in Oncology (preferred) or similar therapeutic area. 
Comprehensive knowledge of ICH GCP, country regulations and all aspects of clinical operational management. 
Clear and accurate communication in written and spoken English. 
Familiarity with the therapeutic areas that are priorities for Company.
Demonstrated ability to interact with different professional levels of the external clinical research community. 
Extensive (≥ 5 years) experience of all phases of clinical development, experience in Oncology drug clinical trial, from Phase I-III, is a must.
Experience of line management of groups, including managing through others and leading high performing multi-functional study teams. 

Competencies
Highly motivated and collaborative, strong communication and interpersonal skills Scientific/Technical excellence. 
Strong ownership and team work spirit with the goal of project delivery. 
Can-do attitude and willingness to take challenge tasks. 
Critical thinking and Problem solving. Ability in working in a complex environment, managing multiple tasks and competing priorities simultaneously.
Ability to work effectively in a changing environment. 
Must be able to manage their own work, highly organized, detail-oriented and able to multi-task with delivering high quality work under strict timelines. 
Decision Making- able to make sound decisions even in the face of ambiguous circumstances or contradictory requirements 
Teamwork and Collaboration- successful and comfortable working in a complex matrix, able to seek common ground in an effort to resolve conflicts, able to pull people together around a common goal, and to build diverse teams leveraging them to deliver exceptional results. 
Cost and financial awareness- good judgment in relation to trade-offs between cost and effectiveness.

其他信息
语言要求:英语、普通话

所属部门:临床部
工作地址
成都-双流区慧谷东一路8号天府国际生物城孵化园D1栋5-8层
公司介绍
四川汇宇制药股份有限公司 企业介绍
四川汇宇制药股份有限公司生产基地位于四川省内江经济技术开发区内,占地面积10万平方米,项目总投资10亿元人民币,致力于高端抗肿瘤药物的研发,生产和销售。公司在四川成都双流区“天府国际生物城”设立全球创新药研发中心,将打造抗体抗癌创新药物研发总部及产业化基地,建设包括从事靶向抗肿瘤小分子化学药和大分子生物药研发、中试及产业化的研发中心,占地面积60亩,规划建筑面积88000平方米,可容纳1500名研发人员,计划在2022年建成运行。
公司以科技创新为导向的发展理念,不断完善小分子化学药物和单克隆抗体生物药物两个技术平台,开发抗肿瘤领域的创新药物,公司一期项目可年产3000万瓶抗癌针剂,实现年产值25亿元人民币。公司的抗癌针剂于2014年通过英国GMP认证,并于同年顺利通过中国GMP认证。2015年7月公司获得欧盟药品放行资质,公司生产的抗癌针剂已经在伊丽莎白女王医院、皇家伦敦医院和剑桥大学附属医院等1200多家欧盟医院作为一线抗癌药物大规模使用。
公司在美国、英国、法国、澳大利亚、加拿大、中国香港等全球80多个国家和地区建立了销售渠道并启动了当地的药品注册工作,已逐步建立并完善遍布全球的销售网络。同时以致力于改善人类健康为崇高宗旨,以‘关爱生命,追求卓越,简单诚信’为价值导向, 力争把公司打造成一家受人尊敬的国际化制药企业。
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