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Project & Program Management

Associate Project Director, Global Regulatory Affairs & Patient Safety

Ascendis Pharma Hellerup, Denmark Posted 1 Oct 2026 Ascendis Pharma CareersSenior specialistEnglish
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Summary

Leads strategic and operational projects across Global Regulatory Affairs and Patient Safety, establishing governance, integrated plans, reporting, and risk management in a global, highly regulated environment.

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Read from the job ad by AI. The employer's own fields always win.

Opportunity summary

Are you passionate about translating strategic priorities into disciplined execution? Do you have extensive experience leading complex, cross-functional projects in the pharmaceutical or biotechnology industry? If so, now is your chance to join Ascendis Pharma as our new Associate Project Director, GRAPS.

Ascendis Pharma is a global biopharmaceutical company committed to making a meaningful difference in patients’ lives. Guided by our core values of Patients, Science, and Passion, we are applying our innovative TransCon® technology platform to fulfill our mission of developing new therapies that demonstrate best-in-class potential to address unmet medical needs.

At our headquarters in Hellerup, Denmark, research facilities in Heidelberg, Germany, and additional offices across Europe and the United States, we are advancing programs in our Endocrinology Rare Disease portfolios. We also collaborate with partners on the development of TransCon-based products in other therapeutic areas and markets.

We are seeking an experienced and highly structured Associate Project Director to join our GRAPS Enablement & Insights function within Global Regulatory Affairs & Patient Safety. In this role, you will translate GRAPS priorities into integrated plans and disciplined execution across Global Regulatory Affairs, Global Patient Safety, and key enterprise functions1 …

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