湖州 [切换城市] 湖州招聘湖州生物/制药/医疗器械招聘湖州生物工程/生物制药招聘

Vx-Medical Affairs Manager-Beijing

赛诺菲中国

  • 公司规模:5000-10000人
  • 公司性质:外资(欧美)
  • 公司行业:制药/生物工程

职位信息

  • 发布日期:2019-07-15
  • 工作地点:北京
  • 招聘人数:1人
  • 工作经验:无工作经验
  • 学历要求:招1人
  • 语言要求:不限
  • 职位类别:生物工程/生物制药

职位描述

JOB PURPOSE:
To provide medical and scientific expertise in the field of Meningitis and be responsible for driving Medical Affairs activities within China region, support the achievement of the highest growth potential of the brands and ensuring coordination and communication between Operating Companies, China and Global organizations in all medical matters. To coordinate with other functions (e.g. Commercial, Regulatory Affairs, Health Economics etc.),to development and presentation of an unified Medical China voice on the Vaccine Development Team (CDT) To manage the development and implementation, by the medical franchise lead, of Medical Affairs Product (MAP) Plans, ensuring close co-operation with Marketing, Regulatory and alignment with Global medical strategy.
KEY ACCOUNTABILITIES:
Therapeutic Area Medial Strategy Responsible to develop and champion a medical strategy and vision for including full lifecycle management, and encompassing pre-marketing activities Responsible for validating franchise strategy with Key Opinion Leaders(KLOs) Responsible for new product development MA plans, which covering study design, etc. Accountable for developing and maintaining annual budget requests and ensuring that individual product budgets are being managed and tracked
Therapeutic Area Medical Representation point of contact(e.g. for coordination of relationships with external alliances/licensing business partners, and for facilitating interactions with interfacing functions) Build internal/external reputation as MA expert, act as a China Provide medical insight and support to China business development initiatives as appropriate Provide China medical expertise and input in global MA and ensure appropriate involve into CDTs Provide medical expertise value into relevant clinical components of China regulatory submission as necessary, and support commercial and New Product Teams where appropriate Responsible for overseeing major medical safety and product issues Internal & external network/KOL management
Develop KOL management strategy and plan in collaboration with other functions
Build an internal and external reputation as expert participating in appropriate professional organizations and meetings.
Product Safety and Regulatory
职位要求:
Requirements
To manage Product-related medical safety issues for provide input to the Area compliance person
Study Planning and Execution
To ensure that all protocols are in alignment with , and support, the medical strategy
Accountable for development of study concepts and scientific content for protocols
Accountable for the preliminary internal and external approval of the Final Study report for all studies
To ensure that clinical study are published and accordance with China and global publication strategy
Medical Education
Develop and conduct lectures/educational sessions for HCP
Conduct training for internal audiences
Consult in the selection and development of expert speakers
Others
Additional scope of responsibilities and other therapeutic areas may be assigned by the Medical Lead
JOB-HOLDER ENTRY REQUIREMENTS:
Education:
-Master degree is preferred
Experience & knowledge:
-At least 5 years industry/business experience with a minimum of 3 years’ experience in a relevant area for this function (e.g. Medical Affairs or Clinical R&D, academic or hospitals)
-Experience and advocacy within a vaccines field is a plus
Core competencies:
-Fluent in English
-Good knowledge of study execution, benefit risk management and regulatory affairs
-Excellent medical science knowledge of in general including main competitors
-In-depth knowledge of study methodology, study design, data review and analysis
-Excellent knowledge of study publication processes and publications
-Strong understanding of the pharmaceutical business
-Good knowledge of all compounds with in depth knowledge of at least one compound

公司介绍

赛诺菲集团
赛诺菲集团是一家全球领先的多元化医药健康企业,专注于患者需求,传播健康。
 全球100,000余名员工,业务遍及100个国家
 新兴市场实力均衡,表现强劲,位列***
 多元领域,覆盖处方药、健康药业产品、疫苗和动物保健品
 疫苗领域的领导者
 领先动物保健市场
 2011年集团净销售额达334亿欧元

赛诺菲在中国
赛诺菲是首批在中国开设办事处的跨国制药集团,也是国内增长最快的医药健康企业之一。目前,赛诺菲在中国200多个城市拥有6000余名员工。
   
传承悠久历史、持续开拓进取
赛诺菲一直以来秉承对中国的承诺。1982年,赛诺菲成为首批在中国开设办事处的跨国制药企业之一。今天,赛诺菲已跻身中国医药健康市场的领军企业。赛诺菲的中国总部位于上海,并在北京、天津、沈阳、济南、上海、杭州、南京、武汉、成都、广州和乌鲁木齐共设11家区域办公室。

独特的医药健康产品系列、满足中国公共卫生需求
从预防到治疗,赛诺菲全方位满足中国的公共健康需求。集团的疫苗事业部赛诺菲巴斯德是中国领先的疫苗企业。赛诺菲在心血管/血栓、糖尿病、肿瘤、内科和中枢神经系统等关键的治疗领域拥有领先产品。2010年,杭州赛诺菲民生健康药业有限公司的成立标志着赛诺菲进入中国的非处方药市场。2011年2月,赛诺菲完成了对BMP太阳石的收购。

大幅投资工业建设、满足中国市场需求
赛诺菲目前在中国拥有六家生产基地,包括北京制药工厂、杭州制药工厂、杭州赛诺菲民生健康药业工厂、南昌梅里亚动物保健工厂、深圳赛诺菲巴斯德疫苗工厂、以及唐山健康药业工厂。

完善的研发架构、双赢的研发合作模式
在中国,赛诺菲具有从药物靶点发现到后期临床研究的整体研发实力。集团在上海设有中国研发中心和亚太研发中心,并在北京和成都分别设有研发机构。自2008年以来,赛诺菲与中国权威科研机构开展了10多项战略合作,在癌症、干细胞、糖尿病和老年疾病等前沿研究领域探索创新药物

依托于强劲的研发能力和多领域领先水平的广泛的医药产品资源,公司在中国的市场份额不断攀升,公司规模不断扩大,飞速发展的业务给了我们与更多优秀人才合作的机会。

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联系方式

  • 公司地址:地址:span北京