Associate Medical Director, Clinical Development - Job ID: 1912, 1913, 1914

Ascendis Pharma is a dynamic, fast-growing global biopharmaceutical company with locations in Denmark, Europe, and the United States. Today, we're advancing programs in Endocrinology Rare Disease and Oncology. Here at Ascendis, we pride ourselves on exceptional science, visionary leadership, and skilled and passionate colleagues. Guided by our core values of Patients, Science, and Passion, we use our TransCon® drug development platform to fulfill our mission of developing new and potentially best-in-class therapies to address unmet medical needs. Our culture fosters a place where skilled, adaptable, and highly resourceful professionals can truly make their mark. We offer a dynamic workplace for employees to grow and develop their skills. The Associate Medical Director is involved in the design, safety monitoring, and data analysis of the Company’s late-phase clinical trials in endocrinology. As such, the Associate Medical Director is an important and visible member of the clinical development team. The Associate Medical Director position is based in the United States, and will report to a Senior Medical Director, Clinical Development. Key Responsibilities Leverage medical expertise and hands-on clinical experience to promote relevance and rigor of the development program For clinical trials: design, provide medical oversight, and support site and subject retention Serve as a Medical Monitor for clinical trials, ensure study integrity, and track accumulating safety and efficacy data Provide leadership to study teams Ensure successful completion of trial-related documents (including clinical trial protocols, investigator brochures, medical monitoring plans, site training materials, clinical study reports, health authority responses, standard operating procedures, etc.) with cross-functional team members Anticipate obstacles within a clinical trial, and implement solutions Analyze, evaluate, interpret, and report study results Contribute to drafting and reviewing clinical documents, manuscripts, presentations, and regulatory submissions Contribute to design of the Clinical Development Plan Maintain up-to-date knowledge of relevant science, medical information, good clinical practices, and regulatory guidance Collaborate with—and serve as a clinical research resource for—cross-functional colleagues to optimize product development Cultivate relationships with investigative sites, clinical consultants, and key opinion leaders to represent the interests of the company Contribute to corporate strategic and organizational initiatives Assist with commercial activities as needed Complete assigned tasks thoroughly, accurately, and on time Adhere to rigorous ethical standards Travel up to 20% domestically and internationally for scientific meetings