Magnet.me  -  Het slimme netwerk waarop hbo‑ en wo‑studenten hun baan of stage vinden.

Het slimme netwerk waarop hbo‑ en wo‑studenten hun baan of stage vinden.

Global Program Regulatory Director

Geplaatst 29 jun. 2024
Delen:
Werkervaring
0 tot 7 jaar
Full-time / part-time
Full-time
Functie
Soort opleiding
Taalvereiste
Engels (Vloeiend)

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Major accountabilities: Regulatory Strategy & Submissions With multiple stakeholders, develop, document and communicate high quality global regulatory strategies and HA interactions to achieve business objectives. Evaluate and communicate potential global regulatory opportunities and risks, developing mitigation strategies Leverage regional expertise in executing global regulatory strategy, and HA engagement. Provide strategic regulatory input into analysis and interpretation of scientific data, to key documentation, Leverage scientifc knowledge and acumen in the analysis, interpretation and communication of data to colleagues. Lead interactions with Regulatory Affairs and Development Unit management and external consultants, for input to regulatory strategies. Accountable, in conjunction (with regulatory labelling) for maintaining Novartis core product information documents though product life cycle. Contribute to any BD&L Due Diligence activity Regulatory Excellence & Compliance Ensure compliance with global regulatory requirements and adherence to regulatory internal policies and processes, coordinating regulatory compliance activities at a global level. Provide support as needed for non-project related excellence activities. People As an effective matrix leader, provide feedback and mentor team members, line functions and sub- teams. Working with line managers, you will provide opportunities for team member growth and development, leading by example acting as a role model for Novartis values and behaviours. Your Experience: Science based bachelor's or master's degree. Advanced degree desirable. Significant regulatory and pharmaceutical development experience, across Phases I-IV. A track record of working with HA guidance and feedback, discussion and negotiations; post marketing/ brand optimization strategies and regulatory operations. Proven leadership success across a broad range of regulatory and pharmaceutical development activities. Strong interpersonal skills and experience working in a complex, cross functional organization, navigating complexity and leading cross function teams. Fluency in English. Why Novartis: Helping people with disease and their families takes more than innovative science. It takes a community of smart, passionate people like you. Collaborating, supporting and inspiring each other. Combining to achieve breakthroughs that change patients’ lives. Ready to create a brighter future together?: https://www.novartis.com/about/strategy/people-and-culture Commitment to Diversity & Inclusion: Novartis is committed to building an outstanding, inclusive work environment and diverse team’s representative of the patients and communities we serve. Join our Novartis Network: Not the right Novartis role for you? Sign up to our talent community to stay connected and learn about suitable career opportunities as soon as they come up: https://talentnetwork.novartis.com/network

Our purpose is to reimagine medicine to improve and extend people's lives. We use innovative science and technology to address some of society's most challenging healthcare issues. We discover and develop breakthrough treatments and find new ways to deliver them to as many people as possible. We also aim to reward those who invest their money, time and ideas in our company.

Overig
Amsterdam
Actief in 80 landen
300 medewerkers
40% mannen - 60% vrouwen
Gemiddeld 40 jaar oud