Regulatory Affairs and Clinical Trials

Working at Novo NordiskWe don't wait for change – we drive it. Our goal is to create life-changing medicines for people with chronic diseases.We're a dynamic company in an even more dynamic industry, striving for excellence without fixating on perfection.Our Clinical Operations team plays a vital role in our ambitious drug development program, planning and...

About Novo NordiskWe're a dynamic company in the biopharmaceutical industry, dedicated to driving innovation and making a meaningful impact on patient care.Our commitment to excellence is evident in our research and development efforts, where we strive to move the needle on therapeutic areas like obesity.The RoleWe're seeking a skilled Regulatory Affairs...

Job Description\Novo Nordisk A/S is seeking an experienced Regulatory Affairs Specialist to join our team. The ideal candidate will have a strong background in regulatory affairs and be able to drive the strategic direction of innovative development projects.\Main Responsibilities:\\Execute and drive the regulatory strategy to obtain approvals\Provide...

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...

Key ResponsibilitiesContribute regulatory expertise to global strategies and tacticsDevelop regulatory documentation for submission to Health Authorities globally, e.g., clinical trial applications, briefing packages, paediatric plans, and responses to health authority questionsRepresent Global Regulatory Affairs in global clinical trial teams and other...

Novo Nordisk A/S: Where Passion Meets PurposeWe're a global leader in diabetes care and biopharmaceuticals, driven by a passion for improving lives. Our mission is to make a meaningful difference for people with chronic conditions, and we need talented individuals to join our team and help us achieve this goal.Role OverviewWe're seeking an experienced...

At Novo Nordisk A/S, we are expanding our product and project pipeline in a fast-paced, dynamic environment.We are seeking an engaged Regulatory Affairs Chemistry, Manufacturing and Control (RA CMC) Specialist with expertise in synthetic small molecules to join the Synthetics & Cell Technologies Department in the RA CMC Biotech & Rare Disease area.The ideal...

The role of Trial Manager - Clinical Development at Novo Nordisk A/S offers a unique opportunity to work in a dynamic and rapidly evolving field. As a Global Trial Manager, you will be responsible for coordinating and ensuring timely trial deliverables, monitoring trial progress, and overseeing vendor deliverables.Your key responsibilities will...

Company OverviewNovo Nordisk A/S is a dynamic company in the pharmaceutical industry, driven by innovation and a commitment to patient care. We strive for excellence without fixating on perfection, embracing experimentation and seizing opportunities for growth.Job DescriptionWe are seeking an experienced Regulatory Affairs Specialist to join our Device and...

Category: Reg Affairs & Safety PharmacovigilanceLocation:Søborg, Capital Region of Denmark, DKAre you passionate about clinical trial submissions? Do you possess a talent for overseeing project management and ensuring compliance with global requirements? If so, we have an exciting opportunity for you to join our newly established team of Submission Managers...

Select how often (in days) to receive an alert: Create AlertExpert in Regulatory Affairs - Primary PackagingCategory: Reg Affairs & Safety PharmacovigilanceLocation:Søborg, Capital Region of Denmark, DKAre you ready to take on new challenges in primary packaging development across emerging therapeutic areas and innovative products? Would you like to use...

Join our team as a Clinical Development Project Lead and play a critical role in shaping the future of medicine. As a seasoned professional with expertise in clinical development, regulatory affairs, and medical communications, you will lead projects from start to finish, ensuring seamless execution and timely delivery.You will work closely with...

At Novo Nordisk, we are expanding our product and project pipeline and seeking an engaged Regulatory Affairs Chemistry, Manufacturing and Control (RA CMC) Specialist with expertise in synthetic small molecules to join the Synthetics & Cell Technologies Department. This role provides strategic, tactical, and operational regulatory input to projects.The...

Job DescriptionThe position involves providing strategic regulatory input, assessing risks, and developing mitigation strategies. Key responsibilities may include:Representing Global Regulatory Affairs in various cross-functional teams.Planning, preparing, and leading Health Authority interactions.Developing regulatory documents, including briefing packages,...

About the DepartmentThe Cardiovascular, Kidney, and Alzheimer Disease Clinical Operations area covers the entire spectrum of clinical development activities, from early phase 1 trials to larger phase 3a programs and phase 3b/4 life cycle management activities.Our Goals:To advance ambitious drug development trials within established and new therapeutic...

About the JobWe are seeking a highly skilled Hematology Clinical Trials Lead to join our team in Rare Diseases. As a key member of our Medical & Science department, you will be responsible for leading the development of clinical trials for patients with rare blood disorders.Your Key ResponsibilitiesDevelop Clinical Trial Protocols: You will work closely with...

Job OverviewWe are seeking a highly skilled Regulatory Affairs Specialist to join our team in innovative development within rare diseases.This is an exciting opportunity to become part of a fast-changing field where no two days are alike.The PositionAs a Regulatory Specialist, you will be responsible for setting the regulatory strategic direction in...

Job OverviewWe are seeking an experienced Clinical Operations Lead to join our dynamic global clinical development team at Novo Nordisk A/S. As a key member of this team, you will play a critical role in shaping the future of obesity drug development programs.About the JobIn this role, you will be responsible for the operational start-up and initiation...

About Us">Novo Nordisk A/S is a global leader in the development of new treatments for rare diseases. Our commitment to innovation and excellence has made us a trusted partner for patients, clinicians, and healthcare professionals around the world.">The Role">We are seeking a skilled Global Medical Director to lead our clinical development efforts in...

Do you want to be part of a dynamic global clinical development team that plays an instrumental role in the ambitious obesity drug development programs at Novo Nordisk? Would you like to be part of the development of new drugs to improve the treatment for Obesity?Then you could be our new Clinical Operations Lead. Apply now for a life-changing careerThe...