Global Medical Lead Enterogermina (all genders)
法兰克福, 德国塞纳河畔纳伊, 法国
Milan, 意大利 Permanent 发布日期 Nov. 21, 2024
About the job
The Global Medical Lead works within the cross-functional Opella Global Brand team and contributes to the development of the cross functional brand strategy. Their key responsibility is the development and execution of the global medical strategy.
The Opella Global Medical Lead’s main objectives are to:
Contribute to the development of the global Opella Brand strategy.
Be responsible for development and execution of the Brand medical strategy. This includes scientific data generation publications, scientific engagement and technical document plans.
Develop a key external expert network and establish relationships with relevant scientific organizations.
Contribute to the design and the oversight of Clinical Studies and RWE studies.
Contribute to the clinical part of Common Technical Document.
Opella, the Consumer Healthcare business unit of Sanofi, is the purest and third-largest player globally in the Over The Counter (OTC) & Vitamins, Minerals & Supplements (VMS) market. We have an unshakable belief in the power of self-care and the role it can play in creating a healthier society and a healthier planet. That’s why we want to make self-care as simple as it should be by being consumer-led always, with science at our core. Through our unique and balanced portfolio of more than 100 loved brands, including 15 global and local high-growth challengers such as Allegra, Dulcolax and Buscopan, we deliver our mission: helping more than half a billion consumers worldwide take their health in their hands. This mission is brought to life by an 11,000-strong team, 13 best-in-class manufacturing sites, and 4 specialized science and innovation development centers. We are also proud to be the first major fast-moving consumer healthcare company to achieve B Corp certification.
Join us on our mission. Health. In your hands.
Main responsibilities:
Globally responsible for strategic medical planning for Enterogermina as one of our 6 key global Brands for both Life Cycle Management as well as Innovation projects.
Lead and oversee operational medical activities’ execution in close cross-functional and global/local collaboration.
Use professional & strategic capabilities to identify critical medical insights & use these to guide global Brand decision making.
Ensure an external focus, including regular external interactions with key stakeholders, is prioritized as a key strategic & learning opportunity.
Monitor & evaluate the implications of the evolving body of scientific evidence.
Be the representative Medical Leader in the Global cross functional Brand team.
Promote scientific innovation opportunities across the global, leverage medical/scientific knowledge to develop robust concepts.
Clearly define the desired outcome(s) from prioritized activities defined in the medical strategy and define operational milestones to deliver on these medical commitments.
Key activities include:
Developing medical insights, anticipate trends, identify & execute on science inspired innovation opportunities, product development, life cycle management, medical evaluation of Business Development opportunities, local switch opportunities, scientific endorsement & stakeholder management, risk mitigation. Development of new claims built to on Brand goals.
Design and Oversee Clinical Studies
Be the strategic lead that identifies the need for evidence generation activities.
Be the strategic lead in the development of clinical studies. This includes providing medical expertise for the scientific content such as study strategy, oversight and approval of the protocol, Key Results Memo, Clinical Study Report and for other clinical development activities (e.g. pre-assessment and cluster feasibility, medical review and validation of clinical data, study risk assessment).
Provide appropriate medical input & support for all activities related to clinical studies such as medical training, feasibility, medical review of data, medical information for the study teams and investigators.
Act as the medical reference in the Clinical Study teams, ensuring the medical relevance of the clinical data.
Common Technical Document (CTD)
Coordinate the preparation of the clinical part of the CTD for FDA & EMA submission to ensure contribution will be provided timely (end to end: from kick off to the provision of the final version ready for submission).
Provide medical expertise for the development of the Clinical part of the CTD.
KEY WORKING RELATIONSHIPS
Global Regulatory Affairs
Pharmacovigilance
Science Hub Regional Heads
Scientific Engagement, Communication and Claims Team
Clinical Operations Team
RWE Team
Global Medical Strategy and Operational Effectiveness Team
Local Medical function
R&D
Growth Hub
About you
Experience: Minimum of 5-8 years of experience in the pharmaceutical industry medical or scientific affairs are required, preferably both locally and globally, and experience in clinical development. Knowledge in the consumer healthcare sector, its pharmaceutical products and its strategic development environment is essential as well as substantial experience in medical strategy development and execution.
Soft and technical skills: Knowledge of industry trends and experience in promoting and implementing process improvement initiatives. Excellent communication skills. Good organizational skills and the ability to handle a large workload under pressure and handle tight deadlines. Ability to anticipate and respond to potential problems and opportunities, ability to act as a business partner, highly adaptable, proactive, time- and detail-oriented, and a high level of professionalism, Familiarity in the field of scientific communication and stakeholder engagement, Ability to evaluate complex problems and propose viable solutions. Experience working within an international company with a complex organizational environment and the ability to operate in a matrix team-oriented structure. Ability to work cooperatively with others; the genuine desire to be part of a team and contribute to organizational and team goals. Proficient in international regulations, guidelines, good practices related to pharmaceutical industry standards and practices. Challenger Mindset Pillars:All in one. Together. Keep each other honest. Have each other`s back. Outcome obsessed. Be personally accountable. Driving sustainable impact and results with integrity. Break boundaries. Take thoughtful risks with creativity. Radically simple. Simple for us. Simple for consumers. As it should be. Required Leadership Competencies: Strategic thinking, business acumen, interpersonal relationships, change leadership, personal leadership, drive learning agility.
Education: Medical degree (MD) or pharmaceutical degree preferred and desirable. Scientific/health related degree (PhD, Phar.D.) is acceptable if supported by good experience.
Languages: Fluent spoken and written English an additional language is desirable.
Why choose us?
Bring the miracles of science to life alongside a supportive, future-focused team.
Discover endless opportunities to grow your talent and drive your career, whether it’s through a promotion or lateral move, at home or internationally.
Enjoy a thoughtful, well-crafted rewards package that recognizes your contribution and amplifies your impact.
Take good care of yourself and your family, with a wide range of health and wellbeing benefits including high-quality healthcare, prevention and wellness programs and at least 14 weeks’ gender-neutral parental leave.
PursueProgress. Discover Extraordinary.
Progress doesn’t happen without people – people from different backgrounds, in different locations, doing different roles, all united by one thing: a desire to make miracles happen. You can be one of those people. Chasing change, embracing new ideas and exploring all the opportunities we have to offer. Let’s pursue progress. And let’s discover extraordinary together.
At Sanofi, we provide equal opportunities to all regardless of race, color, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, disability, or gender identity.
Watch our ALL IN video and check out our Diversity Equity and Inclusion actions at sanofi.com!
追寻 发展。探索 菲凡。
进步需要我们每个人的参与——不论其背景、地域、或职业,我们都有一个共同的愿望:创造奇迹。你也可以成为其中的一员。我们不断追求变革,拥抱新思想,探索我们所能提供的一切机会。让我们一起追求进步。共同发现非凡。
在赛诺菲,不分种族、肤色、血统、宗教、性别、国籍、性取向、年龄、公民身份、婚姻状况、残疾或性别认同,我们为所有人提供平等的机会。
观看 “在赛诺菲的一天” ,并在官网 (sanofi.com) 上查看赛诺菲的多元化、公平与包容倡议!
在法国的职位
我们在法国拥有20,000名员工,分布在28处办公地点。他们肩负着相同的使命:将药物和疫苗带给最需要的人。从入职第一天起,您就能参与重要项目,找到职业发展的航向。无论您是研究员还是市场营销人员,我们都将为您提供相应的工具、资源和支持,帮助您不断追求进步。发展您的个人能力,携手具有包容性的团队,一起改变全球数百万人的生活。
体验可能性
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我们的办公地点
我们的员工遍布60多个国家/地区。他们勠力同心,携手共创医疗健康领域的美好未来。无论您在哪里工作,我们的专家都会指导您推动职业发展,您也将能够运用先进的科学技术,取得意义非凡的重大突破。
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勇敢追梦,奔赴美好未来
想要改变自己的生活,乃至改变全球数百万人的生活,该怎么做?加入我们,开启职业新篇章,然后在我们的保驾护航中展翅高飞,并向优秀的人求教,为这份事业做出切实的贡献。
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您和我们相互依存,共同成长
我们精心打造薪酬体系,为您的身心健康、财务健康与社交健康提供全面保障。我们有着海纳百川的包容性团队文化,无论您在哪个岗位,都能展翅高飞。
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心怀梦想,成就一番事业
我们希望您以饱满的热情投入到自己的工作岗位中,给全球数百万人带来美好生活。您的职业发展道路由您自己来掌控。您只管制定目标,我们会提供充足的培训机会和支持,让您得偿所愿。
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Sanofi’s AI Centre of Excellence in Toronto
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Sanofi Canada's Philanthropic Efforts
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Sustainable and Green
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我们的人与文化
我们是首个建立多元化、公平性和包容性(DE&I)委员会的制药企业。我们还建立了“菲常联盟”,为每位员工提供发声的平台。您的声音是我们建设未来道路的重要基石。
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我们的故事
我们关注每一个员工的声音。因为,我们的未来取决于所有员工的付出与努力。正因为他们的助力,我们才能追求远大的理想。
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为什么选择我们?
我们为您提供各种工具、支持和培训机会,帮助您实现自己的目标。我们也希望您充分发挥潜力,帮助我们实现目标:将新药研发到临床治疗的时间减半。
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