International Medical Director - Clinical Development

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Søborg

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!
The position
In this role, you will be medically responsible for clinical trial design, trial conduct, and trials reporting. You will provide support and share your expertise to advance clinical trials and drug development programs.
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.
  • The workplace is our office buildings in Søborg, Denmark. We can support with a mobility package if moving from your home country.
    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.
    About the Department
    In Medical & Science Rare Bleeding Disorders, we are responsible for the planning, execution and reporting of global clinical trials and for medical and scientific support to health authority interactions within the hemophilia portfolio. Our responsibilities include planning and execution of clinical trials, medical and scientific support to health authority interactions, publications, early research activities, presentations, and more. The current M&S departments consist of 9 medical doctors. We are an integrated part of M&S Rare Disease and Advanced Therapies consisting in total of 27 medical doctors and 9 clinical pharmacologists split across 4 teams.
    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: Mogens Gisselbaek, MD at +45 3448 4442.
    Deadline
    2 April 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 19.3.2024, 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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