Do you want to be part of supporting the growth of a biopharmaceutical company that is developing best-in-class therapeutics that address significant unmet medical needs. Ascendis Pharma is committed to support your personal development on our journey towards becoming a leading rare disease company. Ascendis Pharma is looking to hire a full-cycle Talent Acquisition Partner to partner with business leaders to find great candidates for our growing ...
Company Overview. . We are a dynamic, growing biopharma company with offices in Denmark, Germany and the United States. Today, we're advancing programs in Endocrinology Rare Disease, and Oncology. We are committed to making a meaningful difference for patients. Job Summary. . We are seeking approximately 7-8 months of temporary support for PRC coordination to cover a leave of absence. If you have supported Promotional Review Committees and are op...
. The Head of US Medical - Endocrine Medical Affairs will report to the US General Manager with primary responsibility to lead the US Medical Directors and ensure the compliant execution of all medical programs and functions associated with the late-stage development and medical aspects of commercialization of endocrine assets at Ascendis Pharma. In addition to leading the strategy and execution of phase IV (post-marketing, Registry, Early Access...
Job Description. Job Description. Here at Ascendis we pride ourselves in exceptional science, visionary leadership, skilled and passionate colleagues. We are a dynamic, fast-growing biopharma company with offices in Denmark, Germany, and the United States. Today, we’re advancing programs in Endocrinology Rare Disease, Oncology, and Ophthalmology. We are applying our TransCon technology to build a leading, fully integrated biopharmaceutical compan...
Job Description. Job Description. Here at Ascendis we pride ourselves in exceptional science, visionary leadership, skilled and passionate colleagues. We are a dynamic, fast-growing biopharma company with offices in Denmark, Germany, and the United States. Today, we’re advancing programs in Endocrinology Rare Disease, Oncology, and Ophthalmology. We are applying our TransCon technology to build a leading, fully integrated biopharmaceutical compan...
Job Description. Job Description. The Regulatory Affairs (RA) Associate Director, Labeling will be responsible for labeling activities across programs and stages of development, with specific responsibility for the United States and the Americas and supporting global needs as required. The RA Associate Director, Labeling will be overall responsible for ensuring compliance with US regulatory requirements for labeling, and for coordinating internal...
Are you passionate about leading a global cross-functional program team. Do you have extensive experience within project and program management in late-stage drug development. If so, now is your chance to join Ascendis Pharma as our new Global Program Director for The Endocrine Rare Disease (ERD) Program Management Group. Ascendis Pharma is. a fast-growing biopharmaceutical company with locations in Denmark, Germany, and the United States. We are...
The Director, Regulatory Affairs will be responsible for developing and implementing global regulatory strategies encompassing clinical, non-clinical and CMC disciplines. Provides expertise in translating regulatory requirements into practical, workable plans for project teams with international participants. May mentor and potentially supervise other regulatory professionals working on the project team and regulatory process-related topics. Requ...
This role is involved in the design, monitoring, and data analysis of the Company’s oncology clinical trials. As such, the Associate Director, Oncology Clinical Scientist is an important and visible member of the Oncology team. . Key Responsibilities. Provide input to protocol design, provide oversight of clinical data (entry by sites, data completeness/accuracy working closely with ClinOps/Biometrics/Data Management teams), and support site and ...
The Regulatory Affairs (RA) Associate Director, Labelling will be responsible for labelling activities across programs and stages of development, with specific responsibility for the United States and the Americas and supporting global needs as required. The RA Associate Director, Labelling will be overall responsible for ensuring compliance with US regulatory requirements for labeling, and for coordinating internal labelling activities and proce...
The Sr. Manager, US Marketing will be responsible for developing and executing marketing strategies and tactics for our pharmaceutical products. This role requires the ability to be both strategic and tactical, demonstrating strong leadership, project management, and communication skills. The Sr. Manager reports to Senior Director, US Marketing. This is a hybrid role with 3 days a week working in the Princeton, NJ office and 2 days/week at home. ...
The Senior Manager, Statistical Programmer will be expected to provide timely support to the study team on all programming matters according to project strategies. This role is focused on supporting Oncology team. The incumbent should have hands-on skills and experiences in implementing and executing the programming and project standards to support in production or validation of CDISC SDTM, ADaM datasets, and Tables, Listings, Figures for clinica...
