北京相关职位: 医疗器械销售助理 Japan PV Safety Data Specialist 医院代表-PSR-北京 医药地区经理 医疗器械学术推广 临床监查员CRA实习生 临床监查员CRA实习生 Biostatistician 临床监查员(外派外企CRA) 医学支持
周边城市招聘: 上海 浙江 安徽 广东 山东 河北 重庆 北京 江苏 湖南
企业入驻日期: 2017-11-15
职位描述: Position ProfilePosition Title (Generic): Senior Manager Regional Medical AffairsReports To: Director Global Medical AffairsLocation: BeijingDepartment: R&DPosition 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 tooDevelop strong and persuasive responses to Medical, Scientific and Regulatory questionsoContribute to marketing campaigns that optimise claims opportunities while being compliant with the various regional regulations on advertising, copy clearance, claims generation and justificationoSupport the local / regional business to develop optimal product application strategies to maximise the opportunity for the business post-launchoDevelop and implement global best practices to support and grow the business, drive excellence in operational standards, process and deliveryoDevelop and implement medical strategies for the most relevant local categories and brandsoProvide medical perspective on all key medical matters for Healthcare, including major new development ideas and acquisition opportunities locally / regionallyoSupport all aspects of product development and maintenance/lifecycle management in the local / regional marketoDevelop and leverage strong relationships with external legislative bodies including Regulatory Authorities and KOLsoWork 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 globallyoWork 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 viewoAct as contact person for any external queries as regards medical / scientific aspects of appropriate RB productsoProactively support the project teams, providing medical input and strategic advice to ensure the feasibility and success of product development initiatives within marketoProvide ideas/concepts for constructing the product pipeline (e.g. new products, OTCswitch candidates, new combinations, new technologies) relevant to the local marketoProactively 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.oServe 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 opinionoProvide medical advice to project teams regarding new clinical data or medical press coverage that may impact upon the successful completion of a projectoConduct fair-balanced assessment of efficacy and safety data and provide advice on the best medical approach to drive local brand growthoAssist in registration and development of RB Global products within China and other markets as neededoServe as medical lead for governance activities and collaborate with cross-functional team to develop policies and procedures applicable to the OTC healthcare industry.oServe as regional medical lead for regulatory meetings with CFDA and other regulatory agencies as neededoProvide medical input for development of effective clinical programs in support of local brands as neededoSupport product marketing and R&D teams in creating scientific and medical communicationoCreate and deliver strategic communication plan(s) (e.g. abstracts, posters, review papers, product kits, journal articles)oProvide 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 smoothcooperation 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
北京市朝阳区东大桥路9号侨福芳草地大厦D座6层
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
SCRA/CRA 0.6-1万/月
临床试验助理CTA 0.5-1万/月
制剂专员(化学3类新药) 6-8千/月
新药质量分析实验员 3-4.5千/月
设备维修工 3-4.5千/月
项目主管(3类化药) 6-8千/月
QA质量监控员 3-4.5千/月
高级地区经理 0.8-1万/月
QC分析实验员 3-4.5千/月
制剂车间生产技术员 4.5-6千/月
多肽合成研究员 0.7-1万/月
商务医学专员 4.5-6千/月
临床研究项目经理(医药类) 1.5-2万/月
市场推广专员/活动策划专员 (职位编号:01020) 4.5-6千/月
制剂高级研究员 0.7-1.1万/月
北京相关职位: 医疗器械销售助理 Japan PV Safety Data Specialist 医院代表-PSR-北京 医药地区经理 医疗器械学术推广 临床监查员CRA实习生 临床监查员CRA实习生 Biostatistician 临床监查员(外派外企CRA) 医学支持
周边城市招聘: 上海 浙江 安徽 广东 山东 河北 重庆 北京 江苏 湖南
企业入驻日期: 2017-11-15