Regulatory Data Manager

About the TeamOur Digital Transformation team is responsible for driving change within the RQ&C organisation to optimise and digitalise processes within and across the five areas. We collaborate with internal and external partners regarding projects within the fields of IT & Automation, Process Optimisation, and Data Analytics and Business Intelligence.You...

We are seeking a skilled Data Steward to join our Digital Transformation department at Novo Nordisk. As a key player in this team, you will be responsible for implementing and supporting our data strategy in the Regulatory organisation.Your main responsibilities will include collaborating with cross-functional teams to identify data-related risks and...

At Novo Nordisk, we drive change and strive for excellence in patient care. As a Data Steward, you will play a crucial role in implementing and supporting our data strategy in the Regulatory organisation, ensuring alignment with digital transformation efforts.The ideal candidate will have a strong focus on quality and a 'right first time' mindset, with...

Take on the role of Regulatory Document Preparation Specialist at Novo Nordisk A/S and play a crucial part in driving the preparation of complex clinical documents that meet regulatory requirements.About UsNovo Nordisk A/S is a leading healthcare company focused on defeating diabetes and other serious chronic conditions. We value continuous learning, being...

Would you like to be part of the growth of our processes in digital transformation and bring our new products to our patients faster? Do you want to increase efficiency to accommodate scaling of our business? If yes, we are seeking an experienced and highly motivated Data Steward to join our team, who will be responsible for implementing and supporting our...

Job Description:We are seeking a highly experienced and visionary leader to spearhead our Regulatory Life Cycle Management efforts. As the Director of Regulatory Affairs, you will play a pivotal role in shaping the future of our regulatory strategy.Key Responsibilities:Develop and execute comprehensive regulatory strategies for global approvals.Inspire and...

Select how often (in days) to receive an alert: Create AlertAre you an experienced Medical Writer looking for possibilities to grow your career further and apply your competencies in a global healthcare company? If yes, then we would love to hear from you.At Novo Nordisk, we have a passion for improving patients' lives all over the world. If you want to help...

Overview:This is an exceptional opportunity for a purpose-driven and business-minded second-line leader to join our team and contribute to driving change and innovation in the pharmaceutical industry.Responsibilities:Lead and develop teams responsible for regulatory CMC strategies, driving excellence in our pipeline, and delivering regulatory...

Novo Nordisk A/S is seeking a highly skilled Regulatory Affairs Professional to join our team. In this role, you will play a key role in ensuring the success of our regulatory submissions and approvals. You will work closely with scientists and Health Authority regulators to ensure the smooth execution of regulatory activities, focusing on the creation,...

Global Regulatory Affairs CMC SpecialistWe are seeking a highly skilled Regulatory Affairs Chemistry, Manufacturing and Control (RA CMC) Specialist to join our team in a fast-paced, dynamic environment.As a CMC Regulatory Specialist, you will provide strategic, tactical, and operational regulatory input to projects. You will lead activities for synthetic...