Global Regulatory Strategy Lead for Novo Nordisk

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...

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...

Select how often (in days) to receive an alert: Create AlertCategory: Reg Affairs & Safety PharmacovigilanceLocation: Søborg, Capital Region of Denmark, DKWe are expanding our product and project pipeline in Novo Nordisk and are looking for an engaged Regulatory Affairs Chemistry, Manufacturing and Control (RA CMC) Specialist with expertise in synthetic...

Select how often (in days) to receive an alert: Create Alert (Senior) Regulatory Affairs Professional, RA Obesity - Maternity cover Category: Reg Affairs & Safety Pharmacovigilance Location: Søborg, Capital Region of Denmark, DK Do you have a talent for navigating complex regulatory landscapes and driving strategic initiatives? Are you eager to contribute...

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...

As a seasoned expert in market access and pricing, you will be responsible for developing and executing global pricing strategies for Novo Nordisk's products. This involves leveraging your analytical abilities to estimate price elasticities, assess willingness to pay, evaluate portfolio dynamics, estimate opportunity costs, and determine financial...

Are you passionate about working with data? Do you want to set directions and deliver results? Do you have the ability to handle complex tasks? If yes, we are seeking an experienced and highly motivated Regulatory Data Partner to join our team, who will be responsible for implementing and supporting our data in the Regulatory organisation, and support...

Job DescriptionThis role offers a unique opportunity to join a dynamic team in a fast-paced, global environment. As a CMC Regulatory Specialist, you will play a critical role in ensuring the successful development and approval of our synthetic small molecule projects. Your expertise in regulatory affairs, combined with your knowledge of synthetic small...

Company Overview">Novo Nordisk A/S is a leading global healthcare company with a 100-year legacy of driving change to defeat serious chronic diseases. We recognize the importance of the unique skills and perspectives our people bring to the table, and we work continuously to bring out the best in them.We craft and lead commercial device projects and...

Novo Nordisk A/S is seeking a highly skilled Global Pricing Associate Director to join its team. As a key member of the Global Pricing function, you will play a crucial role in driving the company's commercial success by developing and executing global pricing strategies for all assets.The successful candidate will possess a deep understanding of the...

Job DescriptionWe are seeking a Senior Medical Writer - Regulatory Documents to join our Clinical Reporting team. The successful candidate will have a master's degree within natural sciences, preferably supplemented with a PhD and/or relevant experience in the pharmaceutical industry.Key responsibilities include:Planning, development, and oversight of...

About the RoleNovo Nordisk A/S is seeking an experienced Regulatory Affairs Process Excellence Manager to join our RA Process and Digital Strategy area. As a key member of the team, you will play a central role in driving process excellence, innovation, and digital transformation across the regulatory affairs organization at a corporate level and across all...

Global Associate Director - Device Strategy & Marketing (12-month assignment)Category: Project Management & AgileLocation: Søborg, Capital Region of Denmark, DKOne of our Global Associate Directors is going on a 12-month short term assignment in another function, so now there is a unique opportunity for a 12-month assignment in Device Strategy &...

Global Associate Director - Device Strategy & Marketing (12-month assignment) Category: Project Management & Agile Location: Søborg, Capital Region of Denmark, DK One of our Global Associate Directors is going on a 12-month short term assignment in another function, so now there is a unique opportunity for a 12-month assignment in Device Strategy &...

Select how often (in days) to receive an alert: Create Alert Category: Reg Affairs & Safety Pharmacovigilance Location: Søborg, Capital Region of Denmark, DK Are you an expert in process optimisation? Can you drive strategy, manage complex projects and lead innovation? Are you ready to play a leading role in driving innovation of the regulatory processes...

Category: Reg Affairs & Safety Pharmacovigilance Location: Søborg, Capital Region of Denmark, DK Join our dynamic team and make a significant impact in the realm of RA Business Compliance. We're seeking a talented individual who can effortlessly unravel complex data challenges, deliver impeccable data transparency, and contribute to enhancing overall...

The Ideal CandidateWe are looking for an experienced Regulatory Affairs Chemistry, Manufacturing and Control (RA CMC) Specialist with expertise in synthetic small molecules to join our team. The ideal candidate will have a Master's and/or Ph.D. degree in life sciences with regulatory CMC experience either from the pharmaceutical industry or from a health...

Company OverviewNovo Nordisk A/S is a dynamic company in the pharmaceutical industry, dedicated to improving patient care. Our team works tirelessly to develop innovative solutions and products that address real-world health needs.About the RoleWe are seeking an experienced Regulatory Data Partner to join our RQ&C Digital Transformation department. As a key...

Jobbeskrivelse Placering Bagsværd, Denmark Jobkategori Procurement Ansøg nu Do you have a strong background in project management and a proven track record in driving change and continuous improvement within category management? Are you skilled at building solid relationships with global internal stakeholders and external partners? If so, we look...

About UsNovo Nordisk A/S is a leading pharmaceutical company committed to improving the lives of patients around the world. Our mission is to drive innovation and digital transformation in the healthcare industry.We are seeking an experienced Data Steward to join our team, who will be responsible for implementing and supporting our data strategy in the...