Senior Manager Medical Affairs, North Asia
利洁时(中国)投资有限公司
- 公司规模:5000-10000人
- 公司行业:快速消费品(食品、饮料、化妆品) 制药/生物工程
职位信息
- 发布日期:2017-12-10
- 工作地点:北京
- 工作经验:无工作经验
- 职位月薪:45-80万/年
- 职位类别:医药技术研发管理人员
职位描述
职位描述:
Position Profile
Position Title (Generic): Senior Manager Regional Medical Affairs
Reports To: Director Global Medical Affairs
Location: Beijing
Department: R&D
Position Summary:
Briefly summarize the primary objectives of this position: (Why does it exist)
Regional Medical Affairs Manager is responsible for medical and scientific affairs activities primarily supporting the Health (especially Sexual Wellbeing and Dettol) and the TCM and VMS portfolio within the China/ NA region. In addition, the role will be required to provide medical oversight to other aspects of the NA portfolio as needed. The role provides scientific and medical support for clinical trials, claims substantiation, potential regulatory interaction and all other activities relevant to healthcare specifically. He/she will support ideation, substantiation, and defense of local claims, as well as challenges against competitors' claims. He/she will strengthen the relationship with local key opinion leaders to build up a network of RB advocates for the healthcare category. He/she will support external communication, and provide input to internal / external training. He/she will review and approve promotional Medical-Marketing materials and provide scientific competitive intelligence in China and other markets as needed. He/She will also play a very important role in engaging with Category R&D and other cross-functional global teams to help drive innovation for the China market. The position interfaces with other disciplines within and external to the business, including Category Research & Development (R&D), Global and Local Regulatory Affairs, Healthcare Professional Relations, KOLs and legislative bodies. The role is critical not only in maintaining the day to day ethical, safety and regulatory aspects of the NA healthcare business, but also plays a key role in the medical support for local registration of products within the portfolio.
Responsibilities:
List a series of brief statements describing the end result or major activities of this position. Emphasize the end results rather than individual tasks or steps taken. List in order of their importance.
? Work in collaboration with the commercial operations, Regional R&D, Global and Local regulatory and global medical teams, support the China and other markets as needed to
o Develop strong and persuasive responses to Medical, Scientific and Regulatory questions
o Contribute to marketing campaigns that optimise claims opportunities while being compliant with the various regional regulations on advertising, copy clearance, claims generation and justification
o Support the local / regional business to develop optimal product application strategies to maximise the opportunity for the business post-launch
o Develop and implement global best practices to support and grow the business, drive excellence in operational standards, process and delivery
o Develop and implement medical strategies for the most relevant local categories and brands
o Provide medical perspective on all key medical matters for Healthcare, including major new development ideas and acquisition opportunities locally / regionally
o Support all aspects of product development and maintenance/lifecycle management in the local / regional market
o Develop and leverage strong relationships with external legislative bodies including Regulatory Authorities and KOLs
o Work closely with, advise and influence Professional Relations, Marketing, Regulatory, R&D, Supply and Global Quality, providing medical advice to maintain compliance and help to maximise commercial opportunities locally and globally
o Work closely with the business Quality functions, ensuring internal cross-functional systems and processes are robust to ensure compliance of the broad range of licences products on the market, supporting any GxP or quality issues from a scientific / medical point of view
o Act as contact person for any external queries as regards medical / scientific aspects of appropriate RB products
o Proactively support the project teams, providing medical input and strategic advice to ensure the feasibility and success of product development initiatives within market
o Provide ideas/concepts for constructing the product pipeline (e.g. new products, OTC
switch candidates, new combinations, new technologies) relevant to the local market
o Proactively liaise with external key opinion leaders to enhance the Company's knowledge base. Input relevant information to the project teams to influence strategic project direction.
o Serve as the medical product expert for local and global brands within China and other markets as needed and develop in-depth understanding of the literature and current medical opinion
o Provide medical advice to project teams regarding new clinical data or medical press coverage that may impact upon the successful completion of a project
o Conduct fair-balanced assessment of efficacy and safety data and provide advice on the best medical approach to drive local brand growth
o Assist in registration and development of RB Global products within China and other markets as needed
o Serve as medical lead for governance activities and collaborate with cross-functional team to develop policies and procedures applicable to the OTC healthcare industry.
o Serve as regional medical lead for regulatory meetings with CFDA and other regulatory agencies as needed
o Provide medical input for development of effective clinical programs in support of local brands as needed
o Support product marketing and R&D teams in creating scientific and medical communication
o Create and deliver strategic communication plan(s) (e.g. abstracts, posters, review papers, product kits, journal articles)
o Provide medical support and oversight for promotional activities:
? Provide medical information and advice in the development of promotional claims, ensuring that claims are medically accurate, fair, balanced and defendable in the event of a competitor challenge;
? Liaise with Marketing teams and advertising agencies to maximize promotional claims;
? Review HCP and consumer research proposals, advertising briefs and advertising concepts for new products, providing appropriate medical input and advice.
? Work with Marketing to identify and act upon inappropriate competitor advertising and serve as medical lead in the defense of competitor challenges.
? Ensure that all advice is ethical and legal and within responsibilities covered by medical registration.
Preferred Experience and Skills: Strong medical writing and communication skills as demonstrated through peer reviewed scientific publications and presentations at national and international conferences. Strong collaborative and problem solving skills. Demonstrated project leadership and project management capabilities.
? Has played a lead role in Medical & Scientific Affairs
? Experience in clinical development would be a plus.
? Previous experience in a medical affairs, medical information or product support role. Ideally in an OTC environment.
? Previous experience of work in New Product Development with examples of successful product launches.
? Knowledge and understanding of consumer needs and attitudes, customer groups
(including managed care) and experts advocacy development, as well as smooth
cooperation and teamwork with R&D, Marketing and other internal customers.
Experience in Respiratory Therapeutics category is desired.
? Ability to review and interpret medical and scientific information
? Effective medical and scientific writing skills
Position Profile
Position Title (Generic): Senior Manager Regional Medical Affairs
Reports To: Director Global Medical Affairs
Location: Beijing
Department: R&D
Position Summary:
Briefly summarize the primary objectives of this position: (Why does it exist)
Regional Medical Affairs Manager is responsible for medical and scientific affairs activities primarily supporting the Health (especially Sexual Wellbeing and Dettol) and the TCM and VMS portfolio within the China/ NA region. In addition, the role will be required to provide medical oversight to other aspects of the NA portfolio as needed. The role provides scientific and medical support for clinical trials, claims substantiation, potential regulatory interaction and all other activities relevant to healthcare specifically. He/she will support ideation, substantiation, and defense of local claims, as well as challenges against competitors' claims. He/she will strengthen the relationship with local key opinion leaders to build up a network of RB advocates for the healthcare category. He/she will support external communication, and provide input to internal / external training. He/she will review and approve promotional Medical-Marketing materials and provide scientific competitive intelligence in China and other markets as needed. He/She will also play a very important role in engaging with Category R&D and other cross-functional global teams to help drive innovation for the China market. The position interfaces with other disciplines within and external to the business, including Category Research & Development (R&D), Global and Local Regulatory Affairs, Healthcare Professional Relations, KOLs and legislative bodies. The role is critical not only in maintaining the day to day ethical, safety and regulatory aspects of the NA healthcare business, but also plays a key role in the medical support for local registration of products within the portfolio.
Responsibilities:
List a series of brief statements describing the end result or major activities of this position. Emphasize the end results rather than individual tasks or steps taken. List in order of their importance.
? Work in collaboration with the commercial operations, Regional R&D, Global and Local regulatory and global medical teams, support the China and other markets as needed to
o Develop strong and persuasive responses to Medical, Scientific and Regulatory questions
o Contribute to marketing campaigns that optimise claims opportunities while being compliant with the various regional regulations on advertising, copy clearance, claims generation and justification
o Support the local / regional business to develop optimal product application strategies to maximise the opportunity for the business post-launch
o Develop and implement global best practices to support and grow the business, drive excellence in operational standards, process and delivery
o Develop and implement medical strategies for the most relevant local categories and brands
o Provide medical perspective on all key medical matters for Healthcare, including major new development ideas and acquisition opportunities locally / regionally
o Support all aspects of product development and maintenance/lifecycle management in the local / regional market
o Develop and leverage strong relationships with external legislative bodies including Regulatory Authorities and KOLs
o Work closely with, advise and influence Professional Relations, Marketing, Regulatory, R&D, Supply and Global Quality, providing medical advice to maintain compliance and help to maximise commercial opportunities locally and globally
o Work closely with the business Quality functions, ensuring internal cross-functional systems and processes are robust to ensure compliance of the broad range of licences products on the market, supporting any GxP or quality issues from a scientific / medical point of view
o Act as contact person for any external queries as regards medical / scientific aspects of appropriate RB products
o Proactively support the project teams, providing medical input and strategic advice to ensure the feasibility and success of product development initiatives within market
o Provide ideas/concepts for constructing the product pipeline (e.g. new products, OTC
switch candidates, new combinations, new technologies) relevant to the local market
o Proactively liaise with external key opinion leaders to enhance the Company's knowledge base. Input relevant information to the project teams to influence strategic project direction.
o Serve as the medical product expert for local and global brands within China and other markets as needed and develop in-depth understanding of the literature and current medical opinion
o Provide medical advice to project teams regarding new clinical data or medical press coverage that may impact upon the successful completion of a project
o Conduct fair-balanced assessment of efficacy and safety data and provide advice on the best medical approach to drive local brand growth
o Assist in registration and development of RB Global products within China and other markets as needed
o Serve as medical lead for governance activities and collaborate with cross-functional team to develop policies and procedures applicable to the OTC healthcare industry.
o Serve as regional medical lead for regulatory meetings with CFDA and other regulatory agencies as needed
o Provide medical input for development of effective clinical programs in support of local brands as needed
o Support product marketing and R&D teams in creating scientific and medical communication
o Create and deliver strategic communication plan(s) (e.g. abstracts, posters, review papers, product kits, journal articles)
o Provide medical support and oversight for promotional activities:
? Provide medical information and advice in the development of promotional claims, ensuring that claims are medically accurate, fair, balanced and defendable in the event of a competitor challenge;
? Liaise with Marketing teams and advertising agencies to maximize promotional claims;
? Review HCP and consumer research proposals, advertising briefs and advertising concepts for new products, providing appropriate medical input and advice.
? Work with Marketing to identify and act upon inappropriate competitor advertising and serve as medical lead in the defense of competitor challenges.
? Ensure that all advice is ethical and legal and within responsibilities covered by medical registration.
Preferred Experience and Skills: Strong medical writing and communication skills as demonstrated through peer reviewed scientific publications and presentations at national and international conferences. Strong collaborative and problem solving skills. Demonstrated project leadership and project management capabilities.
? Has played a lead role in Medical & Scientific Affairs
? Experience in clinical development would be a plus.
? Previous experience in a medical affairs, medical information or product support role. Ideally in an OTC environment.
? Previous experience of work in New Product Development with examples of successful product launches.
? Knowledge and understanding of consumer needs and attitudes, customer groups
(including managed care) and experts advocacy development, as well as smooth
cooperation and teamwork with R&D, Marketing and other internal customers.
Experience in Respiratory Therapeutics category is desired.
? Ability to review and interpret medical and scientific information
? Effective medical and scientific writing skills
职能类别: 医药技术研发管理人员
公司介绍
利洁时是全球500强企业,是全球最大的家用清洁及个人护理消费品公司之一,总部位于英国伦敦。在60个国家运作高品质的家用清洁用品、个人护理用品和药品,产品行销180个国家和地区。我们的历史可以追溯到18世纪:在英国生产面粉的Reckitt和在德国生产工业化学原料的Benckiser。1888年开始,我们已经开始在伦敦股票交易所上市,通过合资,以及有选择性的并购,我们已经成为富时指数前25位的全球性公司。
利洁时在中国的发展一直以生产和推广高品质的家庭清洁和个人卫生护理用品、推动中国健康护理事业的发展目标。作为蜚声国际的跨国企业,利洁时在中国市场生产和销售高质量的知名品牌家庭清洁产品。
开发极具潜力的市场,始终是利洁时公司投资的核心战略之一。1995年利洁时来到中国,在广州成立了第一家合资企业-利高曼(广州)有限公司,1996年与湖北活力28集团合资组建了湖北活力美洁时洗涤用品有限公司,从此扎根荆州,开始了利洁时投资中国市场的历程。随着中国国际地位的提升,在加大投资及完成中国区域资源整合的同时,利洁时更坚定了在中国投资的信心。2006年,在中国成立了利洁时家化(中国)有限公司(利洁时全球全资子公司)。为了使中国区的工厂真正成为国际生产基地,几年来利洁时在中国的投资势头不减,在组织结构调整和人员配备方面更是格外重视。2010年随着利洁时全球收购了SSL集团,利洁时在中国增加了新的产品品牌,工厂以及团队。
目前利洁时中国的品牌有:
Dettol (滴露)
Veet (薇婷)
Finish (亮碟)
Airwick (安悦嘉)
Dosia (巧手)
Durex (杜蕾斯)
Scholl (爽健)
Vanish(渍无踪)
我们以我们自己在这个高度竞争的全球市场中创造的成绩而骄傲,并深刻意识到我们的成功是直接和我们善于接受挑战,充满热情和才华的员工联系在一起的。
想要了解我们更多的历史和信息,请参阅公司网站 www.rb.com
利洁时在中国的发展一直以生产和推广高品质的家庭清洁和个人卫生护理用品、推动中国健康护理事业的发展目标。作为蜚声国际的跨国企业,利洁时在中国市场生产和销售高质量的知名品牌家庭清洁产品。
开发极具潜力的市场,始终是利洁时公司投资的核心战略之一。1995年利洁时来到中国,在广州成立了第一家合资企业-利高曼(广州)有限公司,1996年与湖北活力28集团合资组建了湖北活力美洁时洗涤用品有限公司,从此扎根荆州,开始了利洁时投资中国市场的历程。随着中国国际地位的提升,在加大投资及完成中国区域资源整合的同时,利洁时更坚定了在中国投资的信心。2006年,在中国成立了利洁时家化(中国)有限公司(利洁时全球全资子公司)。为了使中国区的工厂真正成为国际生产基地,几年来利洁时在中国的投资势头不减,在组织结构调整和人员配备方面更是格外重视。2010年随着利洁时全球收购了SSL集团,利洁时在中国增加了新的产品品牌,工厂以及团队。
目前利洁时中国的品牌有:
Dettol (滴露)
Veet (薇婷)
Finish (亮碟)
Airwick (安悦嘉)
Dosia (巧手)
Durex (杜蕾斯)
Scholl (爽健)
Vanish(渍无踪)
我们以我们自己在这个高度竞争的全球市场中创造的成绩而骄傲,并深刻意识到我们的成功是直接和我们善于接受挑战,充满热情和才华的员工联系在一起的。
想要了解我们更多的历史和信息,请参阅公司网站 www.rb.com
联系方式
- 公司地址:徐汇区港汇广场42层 (邮编:200000)