International Medical Director - Clinical Development

at  Novo Nordisk

International Medical Director - Clinical Development
Category: Clinical Development
Location:Søborg, Capital Region of Denmark, DK
Would you like to leverage your medical, scientific, and product development skills within the pharmaceutical industry, while working in a dynamic global environment that is constantly evolving? Do you thrive by utilizing your patient-centric mindset and medical scientific acumen in a multicultural and global setting to develop new groundbreaking therapies for patients with high unmet needs within Rare Bleeding Disorders?
If these characteristics describe you, we invite you to become a part of our team in the role of International Medical Director.
Apply today for a life-changing career!

QUALIFICATIONS

To succeed in this role, we expect you to have:

• University degree as a Medical Doctor and clinical research experience, preferably through a PhD or similar.
• Experience in clinical trial design and execution including authority interactions and working on a regulatory submission is a must.
• Research experience from the pharmaceutical or biotech industry is required.
• Demonstrated experience with stakeholder management and informal leadership from working in a cross-functional project-oriented organization.
• Clinical or research understanding of Hemophilia will be an advantage.
• 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 role 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.

Your key tasks will include:

• As the person responsible for Medical & Science input, you will have a significant impact on the overall project progress 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 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, medical affairs etc

To succeed in this role, we expect you to have:

• University degree as a Medical Doctor and clinical research experience, preferably through a PhD or similar.
• Experience in clinical trial design and execution including authority interactions and working on a regulatory submission is a must.
• Research experience from the pharmaceutical or biotech industry is required.
• Demonstrated experience with stakeholder management and informal leadership from working in a cross-functional project-oriented organization.
• Clinical or research understanding of Hemophilia will be an advantage.
• Fluency in spoken and written English