Regulatory Affairs Specialist for Innovative Medicine Development in Rare Diseases

Job DescriptionThe role of a Regulatory Affairs Specialist for Innovative Medicine Development in Rare Diseases involves driving regulatory strategies to obtain approvals for novel therapies.As a key member of our Global Regulatory Affairs team, you will work closely with cross-functional project teams to develop and implement regulatory plans that meet the...

Select how often (in days) to receive an alert: Create Alert Regulatory Affairs Specialist for innovative development within Rare Disease Category: Reg Affairs & Safety Pharmacovigilance Location:Søborg, Capital Region of Denmark, DK Do you want to become part of an exciting environment where engaged people are committed to gain approval of Novo Nordisk's...

We are seeking an experienced purpose-driven and business-minded second line leader with extensive expertise in drug regulatory affairs to join our team as the Director of Regulatory Affairs for Biologics and Rare Diseases.About the roleAs the Director for RA CMC Biologics & Rare Diseases, you will play a pivotal role in shaping the future of RA CMC. We are...

Job Description:Safety Surveillance Specialist (Senior) Role SummaryWe are seeking an experienced Senior Safety Surveillance Specialist to join our Global Safety team at Novo Nordisk. As a key member of the Safety Surveillance Rare Disease team, you will be responsible for leading and driving safety surveillance activities in development projects related to...

Director of Regulatory Affairs for CMC Biologics & Rare DiseasesCategory: Project Management & AgileLocation: Søborg, Capital Region of Denmark, DKAre 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 growing...

We are looking for a dynamic and visionary leader to spearhead our team as the Director of Regulatory Affairs for Biologics and Rare Diseases.About the positionThe RA CMC organization is growing, and we are strengthening our leadership team with a new Director with strong experience and interest in Regulatory Life Cycle Management.Be accountable for the...

Safety Surveillance and Rare Disease TeamWe are part of Global Safety at Novo Nordisk, where dedicated professionals have global responsibility for the establishment of the product safety profile during clinical development. Our team focuses on handling projects within the rare disease indication from development to post-marketing.In this role, you will be...

Sr. Medical Specialist in Haemoglobinopathies and Rare Diseases - Join our team and make a meaningful impact on the lives of patients with rare blood disorders! As a Senior Medical Specialist, you will be responsible for designing and implementing clinical trials for our assets in haemoglobinopathies.About the TeamYou will be part of our Medical & Science...

We are looking for a talented and motivated individual to fill the role of Director of Regulatory Affairs for Biologics and Rare Diseases.About the responsibilitiesAs the Director for RA CMC Biologics & Rare Diseases, you will be responsible for leading and developing high-performing teams to achieve business objectives and deliver exceptional...

We are committed to finding the best candidate for this exciting opportunity as the Director of Regulatory Affairs for Biologics and Rare Diseases.About the departmentThe newly established RA CMC BRD Development Projects & LCM is one of three areas in RA CMC Biologics & Rare Diseases, which is a VP area organized in the RA CMC & Device organization with 270...

About the RoleWe are seeking a highly skilled Clinical Development Specialist to join our team in Rare Diseases. As a key member of our Medical & Science department, you will be responsible for designing and implementing clinical trials for patients with rare blood disorders.Your Key ResponsibilitiesDesign and Implement Clinical Trials: You will lead the...

Select how often (in days) to receive an alert: Create AlertRegulatory Affairs Business Development DirectorCategory: Reg Affairs & Safety PharmacovigilanceLocation:Søborg, Capital Region of Denmark, DKDo you have experience developing medicinal products and identifying regulatory risks and opportunities? Are you knowledgeable about the drug development...

As a member of the Rare Blood Disorders Market Access and Pricing team at Novo Nordisk, you will play a vital role in supporting best global access of our assets that help people with Haemophilia, sickle cell disease (SCD), and Thalassemia. This requires cross-function collaboration, innovation, and working closely with senior leadership.This position offers...

About the RoleWe are seeking an experienced medical professional to join our team as a Global Medical Manager for Alzheimer's disease. In this role, you will be responsible for driving the worldwide Medical Affairs strategic direction for Alzheimer's disease.As a key member of our team, you will work closely with cross-functional stakeholders in Marketing,...

Job OverviewWe are seeking a talented Global Scientific Manager to join our team in Copenhagen, Denmark. As a key member of our Global Medical Affairs team, you will play a critical role in driving the worldwide strategic direction for Alzheimer's disease treatment.The successful candidate will be responsible for developing and implementing scientific area...

Job Description:We are seeking a highly skilled Regulatory Affairs Specialist to join our team in the Cardiovascular & Chronic Kidney Diseases (CVD/CKD) therapeutic area. As a Global Regulatory Lead, you will be responsible for developing regulatory strategies and executing various regulatory tasks within cross-functional project teams.Your key...

About the RoleIn this exciting position, you will have the opportunity to contribute to the development of new medicines and technologies that address unmet medical needs in rare diseases.Your responsibilities will include executing and driving regulatory strategies, providing expert advice on regulatory science and global development projects, and being...

About the JobThis is an exciting opportunity to join our team as a Global Medical Manager for Alzheimer's disease. As a key member of our team, you will work closely with cross-functional stakeholders in Marketing, Patient Access, Clinical Development, Regulatory, Research and Translational Medicine to develop and execute global strategies for Alzheimer's...

Job OverviewWe are seeking an experienced CMC Regulatory Specialist to join our team in Novo Nordisk A/S. As a key member of our regulatory affairs department, you will be responsible for providing strategic, tactical, and operational regulatory input to projects.The ideal candidate will have expertise in synthetic small molecules and experience working with...

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...