Ascendis Pharma is a global biopharmaceutical company focused on applying our innovative TransCon technology platform to make a meaningful difference for patients. Guided by our core values of Patients, Science, and Passion, and following our algorithm for product innovation, we apply TransCon to develop new therapies that demonstrate best-in-class potential to address unmet medical needs. Ascendis is headquartered in Copenhagen, Denmark, and has additional facilities in Europe and the United States. Please visit ascendispharma.com to learn more.
Open Positions
Healthcare Compliance Senior Specialist
8-10 years of Compliance experience in pharmaceutical industry, strong team player, and entrepreneurial mindset
IT Engineer with architect capabilities
5+ years of experience in a similar role, preferably from a regulated industry
Specialist, EDC & Clinical Programmer
10+ years of experience in EDC clinical trial databases and clinical programming, with a relevant academic degree in life sciences
Manager, Global Medical Affairs Planning & Effectiveness
5+ years of experience in project support, analysis, or operations, with excellent organizational and communication skills
Senior Specialist, Drug Product Packaging
Experience in manufacturing and the pharmaceutical industry, with 10+ years of experience in print production, pre-press, or similar, and excellent English communication skills
Senior Manager, Safety Data Analysis and Reporting
3+ years of experience in patient safety, good expertise in safety data analysis and regulatory compliance
Senior Veeva Configuration Specialist
5+ years of hands-on Veeva Vault configuration experience, Veeva Platform Certified Administrator or similar certification, deep understanding of Vault security models, workflows, lifecycles, and metadata
Payroll Specialist
Relevant academic degree, 5+ years of experience, proficiency in spoken and written Danish, strong communication and analytical skills
Director, Government Pricing (Managed Markets Finance) - Job ID: 1727
10+ years of progressive experience in pharmaceutical finance, pricing, market access, or government programs, with a bachelor's degree required
Clinical Trial Supply Manager
6+ years of experience in clinical trial supply management or GMP/GDP-regulated environment, Master's degree in Pharmacy or similar, proficiency in Microsoft Office, fluency in English and Danish
+37 More Jobs Available!
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