Medical Lead
巴塞罗那, 西班牙 Permanent 发布于 Nov. 25, 2025 申请截止于 Dec. 31, 2025Job title: Medical Lead
Location: Barcelona
% of travel expected: Travel required as per business need, up to 60%
Our ambition: deliver best-in-class enterprise services enabling Sanofi to chase the miracles of science to improve people's lives. Sanofi has been building the foundations of enterprise services over the past few years. With the creation of the global business unit Business Operations two years ago, we have elevated our commitment to innovation and excellence.
An expert leadership team, passionate about leading high performance. We are building for the long term. We bring people together – many of them in our four hub locations around the world - which simplify processes, break down barriers and modernize the way we work in Sanofi.
Our critical success factors:
We have identified three key drivers:
1. Community - Building a vibrant team that will attract and engage talent, with four global hubs.
2. Excellence - Simplifying, standardizing and continuously improving processes to capture synergies, scale effects and productivity improvements.
3. Digitalization - Enabling transparency, data-driven decision-making support, agility and rapid innovation across Sanofi's entire value chain.
About the Job
The Medical Lead Roles for Specialty Care or Vaccines or GenMed will focus on certain Therapeutic Areas (TAs) and are seated in the Medical Tower in Business Operations. They play a pivotal role supporting the global & local teams supporting the portfolio of a respective TA via driving strategic initiatives and innovation, content development, literature review and insights preparation, and strategic planning, operational execution, and cross-functional collaboration for Medical and Communication Operations. The ideal candidate will have a robust background and knowledge in the respective therapeutic area, strong leadership skills, and a commitment to advancing medical knowledge and patient care.
Main responsibilities:
· Provide medical and scientific expertise for clinical development programs.
· Be main medical point of contact for study sites in allocated markets.
· Support for clinical trials and research initiatives.
· Provide ongoing support to investigators for Sanofi studies, including site visits as necessary.
· Work closely with local clinical development teams and clinical study units to establish unparalleled relationships with study sites, facilitating efficient participant enrolment.
· Support the development and implementation of medical strategies.
· Engage with key opinion leaders and healthcare professionals.
· Review and contribute to scientific communications.
· Collaborate and review scientific content creation from Medical hub to ensure scientific accuracy and elevating the impact of our scientific communications for launches.
· Participate in medical education activities. Develop and execute plans to deliver medical education initiatives aligned with the global medical objectives.
· Serve as a scientific center of expertise and point of contact for the allocated markets with limited Sanofi medical presence.
· Collaborate with local medical and commercial teams in allocated markets.
· Develop a robust advocacy program by organizing advisory boards and roundtables to build and reinforce product awareness, gather strategic insights, and foster relationships with key external stakeholders.
· Provide contributions and oversight to content development and lifecycle management by mapping and requesting the content needs aligned with global franchise and country medical roadmaps.
· To localize and customize medical content generated by global teams.
· To ensure compliance with regulatory requirements, internal policies, and industry standards.
· Collaborate cross-functionally with other groups across clinical development, commercial, regulatory, and field medical teams and provide clear medical guidance.
People:
1) Maintain effective relationships with the end stakeholders (Medical, regulatory, pharmacovigilance, commercial, clinical community) within the allocated franchise and product.
2) Interact effectively with stakeholders across all departments 3) Constantly assist the medical regulatory writing and scientific writing team in developing knowledge and sharing expertise.
4) Effectively engage with key external stakeholders and build long-term partnerships.
Performance:
1) Maintain and ensure compliance with regulatory guidelines and ensure timely and high-quality delivery of medical and scientific content.
2) Strong analytical skills to assess information and emerging trends, including social, policy, and access-related information, and incorporate them into medical plans.
Stakeholders:
1) Work closely with stakeholders to have an oversight to all activities related to product Lifecyle management, and their alignment with global franchise and country medical roadmaps.
2) Excellent interpersonal, communication, influencing, and networking skills with the ability to work as part of a cross-functional and multicultural team.
About you
Experience: ≥5 years of experience in international pharmaceutical companies, ≥2 years’ relevant experience in medical affairs, experience in brand planning, evidence generation, clinical research methodologies, and medical communications. Neurology experience is a plus.
Soft skills: Excellent interpersonal, communication, influencing, and networking skills, Stakeholder management; superb communication skills; Strong interpersonal and networking abilities in a cross-functional, multicultural team and ability to work independently and within a team environment.
Technical skills: Advanced problem-solving and analytical skills, Medical operational excellence, time, and risk management skills, Excellent technical (medical) editing and writing skills, Excellent planning and project management skills with the ability to work independently.
Education: Advanced degree in life sciences or pharmaceutical sciences (MD [preferred], PhD, PharmD).
Languages: Excellent knowledge of the English language (spoken and written).
#LI-Hybrid #BarcelonaHub #SanofiHubs
null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!
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我们的产品设计师负责帮助人们提高免疫力,物流专家负责将药物送到需要的人手中,而数据分析师则借助先进的技术改善人们的生活。在医疗健康领域,每一次进步都离不开所有人的努力。您可以自由选择自己的职业发展道路。Gig零工项目将帮助您尝试更多岗位,个性化指导将为您挖掘自己从未被发现的优势。加入我们,开启菲凡的职业发展之路。您到底可以走多远?让我们拭目以待!
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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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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