International Medical Director - Diabetes
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Søborg
Would you like to leverage your life-cycle management skills within the pharmaceutical industry, while working in a dynamic global environment that is constantly evolving? Come join our team of diligent medical doctors in a highly collaborative work setting that fosters trust, promotes wellbeing, and values productivity. We offer opportunities for individual advancement in a stimulating setting, where you can utilize your medical acumen, research inclination, analytical competence, and creative thought process to guide the clinical evolution of groundbreaking therapies. Apply today for a life-changing career!
The position In this role, you will be responsible for designing clinical trial plans that incorporate innovative and digital solutions, as well as overseeing the market approval process for insulin icodec. Your key tasks will include: As the person responsible for Medical & Science input, you will have a significant impact on the overall project plans and strategies as well as regulatory interactions. You will play a leading role in designing clinical trials, providing medical oversight in the trial conduct phase, interpreting and documenting trial results, and supporting submissions to health authorities. You will also have a key role as an author for publications of clinical trial data, as well as engaging in interaction with scientific experts and health authorities to achieve the best possible clinical development programs. You will collaborate with many other professionals including statisticians, pharmacologists, trial managers, etc. The workplace is our office buildings in Søborg but we can also offer flexible working. We do as well support you with a mobility package when moving from your home country.
Qualifications To thrive and succeed, we expect you to have: University degree as a Medical Doctor complemented by a PhD. Clinical and research experience from the pharmaceutical industry is required along with understanding of diabetes and/or kidney diseases would be an advantage. Proven experience in planning and executing phase 3b/4 activities of clinical trials. Previous experience with market authorization submissions, Q&A with health authorities, and label negotiations would be an advantage. Demonstrated experience with stakeholder management and informal leadership from working in a cross-functional project-oriented organization. Fluency in spoken and written English.
On a personal level, it is essential that you have a strong analytical mindset and good communication and training skills. We expect you to be flexible, open-minded, and a dedicated team player ready to take on an informal leadership combined with the ability to guide and motivate colleagues. In addition, you thrive in a global environment of continuous and fast development with a focus on high quality and results.
About the Department
In Medical & Science Diabetes, we are responsible for the planning and execution of global clinical trials and for medical and scientific support to health authority interactions within the Diabetes portfolio. We are instrumental in providing documentation and interpretation of clinical data leading to New Drug Applications (NDAs) and variation applications, periodic safety updates on marketed drugs, and drugs in clinical development, market access and external scientific communication. The department is based in a project-centric organisation, and internally we work in cross-functional teams. Our key external stakeholders are the scientific community and medical experts, regulatory authorities, and market access institutions.
Working at Novo Nordisk
At Novo Nordisk, we don’t wait for change. We drive it. We’re a dynamic company in an even more dynamic industry, and we know that what got us to where we are today is not necessarily what will make us successful in the future. We embrace the spirit of experimentation, striving for excellence without fixating on perfection. We never shy away from opportunities to develop, we seize them. From research and development, through to manufacturing, marketing, and sales – we’re all working to move the needle on patient care. Contact
For further information, please contact Sr. Director: Roman Cailleteau, MD at +45 30 79 67 52. Deadline
18 March 2024 Please refrain from adding a photo to your CV to ensure fair and efficient processing.
By submitting your application for this position, you acknowledge and agree that your CV and application materials may be accessible and viewed by relevant managers within our organization for the purpose of evaluating your candidacy.
We commit to an inclusive recruitment process and equality of opportunity for all our job applicants. At Novo Nordisk we recognize that it is no longer good enough to aspire to be the best company in the world. We need to aspire to be the best company for the world and we know that this is only possible with talented employees with diverse perspectives, backgrounds and cultures. We are therefore committed to creating an inclusive culture that celebrates the diversity of our employees, the patients we serve and communities we operate in. Together, we’re life changing.
The position In this role, you will be responsible for designing clinical trial plans that incorporate innovative and digital solutions, as well as overseeing the market approval process for insulin icodec. Your key tasks will include:
Qualifications To thrive and succeed, we expect you to have:
On a personal level, it is essential that you have a strong analytical mindset and good communication and training skills. We expect you to be flexible, open-minded, and a dedicated team player ready to take on an informal leadership combined with the ability to guide and motivate colleagues. In addition, you thrive in a global environment of continuous and fast development with a focus on high quality and results.
About the Department
In Medical & Science Diabetes, we are responsible for the planning and execution of global clinical trials and for medical and scientific support to health authority interactions within the Diabetes portfolio. We are instrumental in providing documentation and interpretation of clinical data leading to New Drug Applications (NDAs) and variation applications, periodic safety updates on marketed drugs, and drugs in clinical development, market access and external scientific communication. The department is based in a project-centric organisation, and internally we work in cross-functional teams. Our key external stakeholders are the scientific community and medical experts, regulatory authorities, and market access institutions.
Working at Novo Nordisk
At Novo Nordisk, we don’t wait for change. We drive it. We’re a dynamic company in an even more dynamic industry, and we know that what got us to where we are today is not necessarily what will make us successful in the future. We embrace the spirit of experimentation, striving for excellence without fixating on perfection. We never shy away from opportunities to develop, we seize them. From research and development, through to manufacturing, marketing, and sales – we’re all working to move the needle on patient care. Contact
For further information, please contact Sr. Director: Roman Cailleteau, MD at +45 30 79 67 52. Deadline
18 March 2024 Please refrain from adding a photo to your CV to ensure fair and efficient processing.
By submitting your application for this position, you acknowledge and agree that your CV and application materials may be accessible and viewed by relevant managers within our organization for the purpose of evaluating your candidacy.
We commit to an inclusive recruitment process and equality of opportunity for all our job applicants. At Novo Nordisk we recognize that it is no longer good enough to aspire to be the best company in the world. We need to aspire to be the best company for the world and we know that this is only possible with talented employees with diverse perspectives, backgrounds and cultures. We are therefore committed to creating an inclusive culture that celebrates the diversity of our employees, the patients we serve and communities we operate in. Together, we’re life changing.
Information og data
Denne ledige stilling har jobtypen "Forretningsudvikler", og befinder sig i kategorien "Kommunikation, marketing, salg".
Arbejdsstedet er beliggende i Søborg.
Jobbet er oprettet på vores service den 5.3.2024, 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.
- Forretningsudvikler
- Søborg
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