Associate Director, Pharmacovigilance Projects & Collaborations

Are you passionate about patient safety? Do you have experience within post marketing programs and associated PV regulations? If so, now is your chance to join Ascendis Pharma as our new Associate Director, Pharmacovigilance Projects & Collaborations . 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 a passionate Associate Director, Pharmacovigilance Projects & Collaborations lead to join our growing team. As a key member of the Ascendis Pharma team, you will play a crucial role in establishing PV processes in post marketing programs/projects, while ensuring compliance with Global PV regulations. This is an exciting opportunity to work in a fast-paced environment, collaborate with cross-functional, global teams working together to achieve extraordinary results. You will be joining the Pharmacovigilance Vendor Management team consisting of 4 colleagues, and report directly to Peleg Ben-Efraim, Director, head of Pharmacovigilance Vendor Management team, who is based in CA, US. You will be based in Hellerup, Denmark. Your key responsibilities will be: Pharmacovigilance related responsibilities during the initiation, conduct and closure of Organized Data Collection programs for marketed products. These activities include, but are not limited to: Lead pharmacovigilance activities across the lifecycle (initiation, conduct, closure) of Organized Data Collection programs for marketed products, ensuring compliance with global/local regulations and company policies. Partner with internal stakeholders to identify and establish PV processes in Organized Data Collection programs and other activities such as Digital Platforms, Call Centers and more. Provide strategic input to the PV set up and execution in programs, including vendor contracts, AE handling processes, and timelines. Ensure effective oversight and performance of service providers/vendors, including risk identification, monitoring, and CAPA implementation. Oversee the SDQC and CTV activities performed by service providers/vendors, ensuring timely completion and compliance. Collaborate closely with GVP Compliance, Commercial, Medical Affairs, and affiliates to ensure consistent and compliant PV practices globally and locally. Develop, maintain, and own global PV processes (e.g., SOPs) and related training materials;…