Global Regulatory Lead
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Can you take regulatory lead on a very ambitious growth strategy?
If you bring solid RA experience, and you are looking for a job where you are the one to make things happen according to a very ambitious strategy, this job is your perfect match. As part of LEO Pharma’s goal of becoming the world’s preferred der-matology care partner, we want to further develop and bring new opportunities for our portfolio of established products to new markets around the globe – and you will play a significant role as overall responsible for the regulatory strategy of mak-ing this happen. You will lead and execute on the strategies together with your team of dedicated RA Professionals.
Regulatory strategist responsible for delivering global strategies on own portfolio
We have the products. The market is there on a global scale. Now the task is to bring our high quality products to new markets and at the same time ensure we utilise all development and optimisation oppotunitties in existing markets.
You will be the regulatory anchor-person in this exciting journey and overarching responsible for regulatory strategies and de-liverables across Life Cycle Management (LCM) activities of your portfolio.
As GRL you will:
Lead a small team of Regulatory professionals Develop regulatory strategies (including prioritisations opportunities) for global projects together with cross-functional team members in GRTs (global regulatory team). Drive and lead the regulatory agenda in the cross-organisational teams. Steer the planning cycle to ensure right resources at right time and place Represent RA in development and implementation of new business areas and concepts Build relations to RA colleagues and key stakeholders across the global organisation Contribute to the overall development of the RA function in LEO – strategy input etc.
As Regulatory Lead you will but not handle hands-on regulatory work yourself.
Outgoing profile with +10 years’ of regulatory experience
You have a natural science degree and minimum 10 years’ experience within Regulatory Affairs. As such, you bring compre-hensive knowledge on regulatory, guidelines and regulation, related theories and principles as well as solid hands-on expe-rience within various regulatory submissions.
Managerial experience either as project manager or people manger has taught you how to lead, motivate, empower and develop team members, and you have the open-minded approach it takes to build relations and create results across cultural and professional borders.
You will need all of your drive for results including your optimistic and pragmatic yes-can-do attitude that enables you to make people believe in your ideas and support your agenda. As part of this, you meet people with curiosity and a genuine interest in understanding their agendas and prioritisations. Additionally, you have the communication skills to bridge different areas of expertise including the ability to bring in new ideas when it makes sense.
If you bring solid RA experience, and you are looking for a job where you are the one to make things happen according to a very ambitious strategy, this job is your perfect match. As part of LEO Pharma’s goal of becoming the world’s preferred der-matology care partner, we want to further develop and bring new opportunities for our portfolio of established products to new markets around the globe – and you will play a significant role as overall responsible for the regulatory strategy of mak-ing this happen. You will lead and execute on the strategies together with your team of dedicated RA Professionals.
Regulatory strategist responsible for delivering global strategies on own portfolio
We have the products. The market is there on a global scale. Now the task is to bring our high quality products to new markets and at the same time ensure we utilise all development and optimisation oppotunitties in existing markets.
You will be the regulatory anchor-person in this exciting journey and overarching responsible for regulatory strategies and de-liverables across Life Cycle Management (LCM) activities of your portfolio.
As GRL you will:
As Regulatory Lead you will but not handle hands-on regulatory work yourself.
Outgoing profile with +10 years’ of regulatory experience
You have a natural science degree and minimum 10 years’ experience within Regulatory Affairs. As such, you bring compre-hensive knowledge on regulatory, guidelines and regulation, related theories and principles as well as solid hands-on expe-rience within various regulatory submissions.
Managerial experience either as project manager or people manger has taught you how to lead, motivate, empower and develop team members, and you have the open-minded approach it takes to build relations and create results across cultural and professional borders.
You will need all of your drive for results including your optimistic and pragmatic yes-can-do attitude that enables you to make people believe in your ideas and support your agenda. As part of this, you meet people with curiosity and a genuine interest in understanding their agendas and prioritisations. Additionally, you have the communication skills to bridge different areas of expertise including the ability to bring in new ideas when it makes sense.
Information og data
Denne ledige stilling har jobtypen "Produktspecialist", og befinder sig i kategorien "Kommunikation, marketing, salg".
Arbejdsstedet er beliggende i Ballerup.
Jobbet er oprettet på vores service den 7.11.2019, men kan have været deaktiveret og genaktiveret igen.
Dagligt opdateret: Dette job opdateres dagligt ud fra jobudbyderens hjemmeside via vores søgemaskineteknologi og er aktivt lige nu.
- Produktspecialist
- Ballerup
- Søndag den 24. november 2019
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| Dato | Alle jobs som produktspecialister |
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