PM Reg & Med Coordinator
Budapest, Hongrie Permanent Date de publication Sep. 24, 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!
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#SanofiCareers
#PursueProgress
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#joinsanofi
#careerswithpurpose
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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.
Toujours progresser. Découvrir l’extraordinaire.
Le progrès ne se fait pas tout seul, ce sont les gens qui le construisent : des gens d'horizons différents, dans des lieux différents, dans des rôles différents, mais tous réunis par une même motivation : la volonté de rendre l’impossible possible. Et si vous rejoigniez cet élan ? Afin de poursuivre le changement, adopter de nouvelles idées et explorer toutes les opportunités que nous avons à offrir. Ensemble, continuons de progresser. Et partons à la découverte de l'extraordinaire.
Chez Sanofi, nous croyons en l’égalité des chances pour tout le monde, indépendamment de l’origine, de la couleur de peau, des croyances, du genre, de l'orientation sexuelle, de l'âge, de la citoyenneté, de l'état civil, du handicap ou de l’identité de genre.
Regardez « Une journée type chez Sanofi » et découvrez nos initiatives en matière de diversité, d'équité et d'inclusion sur sanofi.com
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