Associate Project Director, Global Regulatory Affairs & Patient Safety

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 functions. You will lead strategic and operational initiatives involving multiple functions, geographies, vendors, and systems, while establishing clear governance, decision pathways, performance reporting, and risk management. This is an exciting opportunity to combine strategic perspective with hands-on project leadership in a global and highly regulated environment. You will work closely with the GRAPS Leadership Team, functional leaders, and cross-functional stakeholders to strengthen quality, compliance, predictability, and organizational scalability. You will join the GRAPS team ( Global Regulatory Affairs & Patient Safety) and report directly to Jethro Ekuta, Chief Regulatory & Safety Officer, who is based in US. The position may be based in US or DK, with travel to Ascendis Pharma locations and other business-critical meetings as required. Your key responsibilities will be: Lead assigned GRAPS projects and programs from initiation through closeout, establishing clear scope, objectives, governance, integrated plans, milestones, accountabilities, dependencies, budgets, risk controls, and measurable outcomes. Partner with GRAPS leaders to translate strategic priorities into roadmaps and sequenced execution plans, while maintaining a consolidated view of the GRAPS project portfolio, including capacity constraints, interdependencies, risks, and decisions requiring leadership attention. Establish and facilitate fit-for-purpose governance, steering forums, workshops, stage reviews, and decision-making processes, and prepare concise executive dashboards, status reports, decision materials, and…