Rare Disease Safety Lead

Job OverviewWe are seeking an experienced safety surveillance specialist to join our team at Novo Nordisk. As a key member of our Global Safety team, you will be responsible for leading safety surveillance activities in development projects for rare diseases.Your primary focus will be on ensuring the safe development and marketing of our products, working...

Job Description:The Director of Regulatory Affairs for CMC Biologics will lead the development and execution of regulatory strategies for biologics and rare diseases. This role requires a seasoned leader with extensive experience in regulatory affairs, able to inspire and empower teams to deliver high-quality results.Key Responsibilities:Develop and execute...

Job SummaryThis is an exceptional opportunity to make a meaningful impact in the realm of rare disease treatment access. As the Global Director for Health Economics & Outcomes Research, you will be at the forefront of pioneering initiatives that shape the way rare disease treatments are perceived, valued, and accessed worldwide.Key responsibilities...

JobbeskrivelsePlacering Søborg, DenmarkJobkategori Market Access Ansøg nu Are you ready to make a meaningful impact in the realm of rare disease treatment access? As the Global Director for Health Economics & Outcomes Research, you will be at the forefront of pioneering initiatives that shape the way rare disease treatments are perceived, valued, and...

Jobbeskrivelse Placering Søborg, Denmark Jobkategori Market Access Ansøg nu Are you ready to make a meaningful impact in the realm of rare disease treatment access? As the Global Director for Health Economics & Outcomes Research, you will be at the forefront of pioneering initiatives that shape the way rare disease treatments are perceived, valued, and...

Category: Reg Affairs & Safety Pharmacovigilance Location: Søborg, Capital Region of Denmark, DK Do you want to lead and drive safety surveillance activities in development projects in rare diseases? And would you like to be part of one of the most skilled and advanced pharmacovigilance functions in Denmark? Then, this might be a great opportunity for you...

About the RoleThe position of Global Director for Health Economics & Outcomes Research (HEOR) at Novo Nordisk A/S is a crucial role in shaping the company's approach to rare disease treatment access worldwide.As a seasoned expert in Health Economics and Outcomes Research, you will lead the development of strategies, plans, and tactics within the HEOR domain....

About the RoleWe are seeking a Senior Clinical Strategist to join our team in Copenhagen, Denmark. As a key member of our clinical drug development team, you will be responsible for developing and executing clinical strategies for our pipeline, collaborating with cross-functional teams, and ensuring timely delivery of projects.Your ResponsibilitiesDesign and...

Job Description:We are seeking an experienced leader to join our team as the Director of Regulatory Affairs for CMC Biologics and Rare Diseases. As a key member of our leadership team, you will play a pivotal role in shaping the future of RA CMC. Your expertise in drug regulatory affairs will drive excellence in our pipeline and deliver regulatory approvals...

About the RoleThe Global Director for Health Economics & Outcomes Research will be at the forefront of pioneering initiatives that shape the way rare disease treatments are perceived, valued, and accessed worldwide.This role entails leading the development of health economic models, collaborating with multiple stakeholders, and working closely with the...

About Novo Nordisk A/SWe are a proud life-science company dedicated to ensuring people can lead a life independent of chronic disease.As the Global Director for Health Economics & Outcomes Research, you will join our dedicated team working to support the best global access to our assets for patients with Haemophilia, sickle cell disease (SCD), and...

Job Summary:The Director of Regulatory Affairs for CMC Biologics will be responsible for developing and executing regulatory strategies for biologics and rare diseases. This role requires a highly experienced and visionary leader who can inspire and empower teams to deliver high-quality results.Key Challenges:Developing and executing global approval...

About the PositionThis role requires a highly skilled professional with experience in safety surveillance and development in the pharmaceutical industry. You will be responsible for leading safety surveillance activities in development projects for rare diseases and working closely with other teams to ensure safe product development and marketing.As a senior...

About Novo Nordisk:Novo Nordisk A/S is a leading global healthcare company with a 100-year legacy of driving change to defeat serious chronic diseases. Our success relies on the joint potential and collaboration of our more than 69,000 employees around the world. We recognize the importance of unique skills and perspectives our people bring to the table.Key...

Medical & Science, Rare Blood DisordersWe are part of Medical & Science, Rare Disease and Advanced Therapies in Clinical Drug Development and situated in Søborg, Copenhagen, Denmark. We are close to the patients and passionate about developing new treatments for rare diseases including blood disorders and we span over various technologies. In your role, you...

Novo Nordisk A/S is a global healthcare company that has been driving change to defeat diabetes and other serious chronic diseases for over 100 years.We employ more than 65,000 bright and diverse minds in 80 offices worldwide. Our treatments today benefit millions of people living with diabetes, obesity, and rare blood and endocrine diseases.As a Senior IT...

Director of Regulatory Affairs for CMC Biologics & Rare Diseases Category: Project Management & Agile Location: Søborg, Capital Region of Denmark, DK Are you an experienced purpose-driven and business-minded second line leader with extensive expertise in drug regulatory affairs? Do you excel in a dynamic environment and want to be part of a rapidly...

About Our TeamWe are a dynamic global clinical development team at Novo Nordisk, where you will play a key role in advancing ambitious drug development trials within the area of Cardiovascular, Kidney and Alzheimer Diseases (CKAD).In this senior role, you will be accountable for end-to-end planning, execution, and completion of global trials. Your main...

About the CompanyNovo Nordisk A/S is a global healthcare company headquartered in Denmark. We have been driving change to defeat diabetes and other serious chronic diseases for 100 years. Our treatments today benefit millions of people living with diabetes, obesity, and rare blood and endocrine diseases.We employ more than 63,000 bright and diverse minds in...

Join Our TeamWe are a global leader in the development of innovative treatments for rare diseases, including blood disorders. Our team of experts is passionate about making a life-changing impact on patients' lives.Key ResponsibilitiesLead the development and execution of clinical strategies for our pipeline, collaborating with cross-functional teams.Design...