PM Reg & Med Coordinator
布达佩斯, 匈牙利 Permanent 发布日期 Nov. 18, 2024PM Reg & Med Coordinator - Sanofi - Budapest
PM Reg & Med Coordinator is responsible for some EU (or Eurasian) markets:
- The coordination of the distributors and/or Third Parties acting on behalf of Sanofi and its subsidiary entities in some EU markets, by providing them with the dossiers to be submitted in these concerned countries with the required guidance and timing and they will provide oversight to ensure the appropriate compliance of their activities as per the Master Service Agreement from a regulatory and medical perspective
- Managing the portfolio of European products (medicinal products (chemically defined and herbal), medical devices, food supplements and cosmetics if applicable) under development and/or marketed products as well as from a medical perspective.
- For global products/projects, they will provide regional Science strategy and are responsible for operational aspects on dossiers´ preparation and submission.
- They will be also responsible to strengthen the regional and local brands by supporting new claims and will be in direct coordination with the global medical teams for the regional execution
KEY ACCOUNTABILITIES
PM Reg & Med Coordinator is responsible for some EU (or Eurasian) markets:
- Manage Distributors/Third Parties to ensure excellent and compliant execution of operations in the concerned markets
- Define, coordinate, and contribute to the preparation of the dossiers and response documents to Health Authority questions within the Science organization for regional and defined multi-regional products/projects.
- Direct Health Authority interaction and communication for European / Eurasian procedures in case needed
- Provide scientific contribution to Risk Management Plans, Periodic Safety Update Reports, Addendum to Clinical and Nonclinical Overview, Core labelling documentation (e.g. Company Core Data Sheets and Core Safety Profiles), etc. for regional and defined multi-regional products/projects
- Provide Science support to policy, external trade association collaboration, and risk management.
- Be accountable for the maintenance of the existing European portfolio, managing the maintenance activities such as renewals, variations, benefit/risk assessments, referrals, discontinuation process, PRAC signals, PBRER/PSUSA etc.
- Ensure compliance of regulatory activities for development and marketed regional products
- Provide scientific support for registration activities in countries outside the Region
- Steer operational excellence coordination and governance within the region to ensure adherence to internal deadlines and KPIs, e.g. monthly validation of events of worldwide CHC medicinal products´ portfolio in accordance with the applicable EU / Eurasian regulations
- Provide regional input for development of the GRPS (Global Regulatory Product Strategy) and ensure timely execution of defined milestones for global development projects as per blue print.
- Follow regulatory changes, competitors’ status and assess potential impact on daily activities and project strategy
- Drive the scientific assessment for the business opportunities from the Innovation Team / Business development
- Oversight of the regulatory data bases and track the missing data in case needed through spontaneous checks and monthly issuing of the KPI reports.
Requirements:
Education
- PhD, PharmD or MD supported by good experience.
Required knowledge and/or experience
- Minimum 2-3 years experience in the Consumer Healthcare or Pharmaceutical industry, in Regulatory Affairs (global, regional, or local)
- Project management experience in the pharmaceutical industry or in an international regulatory environment
- Demonstrated ability to work in a matrix environment and implement operational regulatory excellence
- Comprehensive expert knowledge of and operational expertise in regional pharmaceutical regulations of medicinal products and medical devices as well as food supplements in EU and Eurasia
- Ability to evaluate impact of new regulations within the drug development environment and to lead discussions of the requirements and its impacts within submission teams
Language skills
- Fluent spoken and written English
- A second language is desirable, preferably Russian
When joining our team, you will experience:
- An international work environment, in which you can develop your talent and realize ideas and innovations within a competent team
- An attractive, market-oriented salary and cafeteria benefits
- Flexible home office policy, with a possibility to work up to 60% of time from home / where you can easily schedule your office days
- Work from an "Office of the Year 2020" finalist office
- Collective life and accident insurance
- Yearly medical check-up
- An individual and well-structured introduction and training of new employees and we will dedicate a Buddy for you to better navigate in your first weeks
- Your own career path within Sanofi. Your professional and personal development will be supported purposefully
- Practice your language skills within our "Language Club"
- Join a great community & special events (Monthly Board Game Nights, Summer Events, Well-Being Lectures & Sport Clubs)
Pursue progress, discover extraordinary
Better is out there. Better medications, better outcomes, better science. But 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. So, let’s be those people.
At Sanofi, we provide equal opportunities to all regardless of race, colour, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, ability, gender identity or Veteran status.
Watch our ALL IN video and check out our Diversity Equity and Inclusion actions at sanofi.com!
#Sanofi #WeNeverSettle
#SanofiCareers
#PursueProgress
#DiscoverExtraordinary
#joinsanofi
#careerswithpurpose
#SBSBUDAPEST
#LI-EUR
#LI-CHC
At Sanofi diversity and inclusion is foundational to how we operate and embedded in our Core Values. We recognize to truly tap into the richness diversity brings we must lead with inclusion and have a workplace where those differences can thrive and be leveraged to empower the lives of our colleagues, patients and customers. We respect and celebrate the diversity of our people, their backgrounds and experiences and provide equal opportunity for all.
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!
共享中心
从波哥大到布达佩斯,从吉隆坡到海得拉巴,我们的版图上处处都有您的全力付出。如果您选择在共享中心施展抱负,您将身处全球变革的中心。我们无惧艰难,并肩作战,努力缩短新药抵达患者手中的时间。您将充分发挥创造力,成就独一无二的自我,从而帮助其他人拥有健康生活。让我们努力探索先进科技,改变更多人的生活。
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
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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
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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。