Global Regulatory Specialist Obesity

Select how often (in days) to receive an alert: Create Alert Regulatory Affairs Specialist, RA Obesity Category: Reg Affairs & Safety Pharmacovigilance Location: Søborg, Capital Region of Denmark, DK Are you passionate about regulatory science and driving innovative regulatory strategies to bring innovative medicines to patients? Do you have strong...

Job OverviewWe are seeking a Global Medical Lead for Obesity to join our team. As part of this role, you will be responsible for leading the planning and design of clinical studies, providing medical oversight during study conduct, and interpreting data to inform regulatory submissions.About the Team:Our Medical & Science team is passionate about advancing...

About Novo Nordisk A/SWe are a dynamic company in an even more dynamic industry, always striving to drive change and move the needle on patient care.Our team is responsible for developing and executing global regulatory strategies, advancing projects across multiple indications from early development through worldwide submission and approval.As a Global...

Job DescriptionWe are seeking an experienced Medical Director to lead our Obesity team in driving the planning and design of clinical studies. The successful candidate will provide medical oversight during study conduct, collaborate with cross-functional teams, and interpret data to inform regulatory submissions.Key Responsibilities:Drive the planning and...

Select how often (in days) to receive an alert: Create Alert Medical Doctor for Obesity Clinical Development Category: Clinical Development Location: Søborg, Capital Region of Denmark, DK Are you a medical doctor with experience and passion for clinical drug development and a flair for thinking strategically? Is designing and executing clinical trial...

About the Role:We are seeking a highly skilled Regulatory Affairs Business Development Director to join our team at Novo Nordisk A/S. As a member of our Regulatory Affairs Diabetes and Obesity team, you will play a pivotal role in creating global regulatory strategies to advance projects from the early stages of development to worldwide submissions and...

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...

Select how often (in days) to receive an alert: Create Alert Regulatory Affairs Business Development Director Category: Reg Affairs & Safety Pharmacovigilance Location: Søborg, Capital Region of Denmark, DK Do you have experience developing medicinal products and identifying regulatory risks and opportunities? Are you knowledgeable about the drug...

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...

About the RoleWe are seeking an experienced Regulatory Affairs Chemistry, Manufacturing and Control (RA CMC) Specialist with expertise in synthetic small molecules to join our team. As a key member of our regulatory affairs department, you will provide strategic, tactical, and operational regulatory input to projects. Your responsibilities will include...

Key ResponsibilitiesAs a Regulatory Affairs Business Development Director at Novo Nordisk, you will be responsible for:Leading RA BD activities and establishing a Matrix Team covering all relevant regulatory skill areas.Evaluating external assets and companies for in-licensing, partnerships, or acquisitions across Novo Nordisk's therapeutic...

About the RoleSafety Surveillance is a key function within Global Safety at Novo Nordisk, responsible for establishing the product safety profile during clinical development and performing critical analysis and medical evaluation of emerging aggregate safety data.We are looking for a skilled Safety Surveillance Expert to join our Obesity team. As a key...

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 Category: Reg Affairs & Safety Pharmacovigilance Location: Søborg, Capital Region of Denmark, DK We 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...

Key ResponsibilitiesApplying regulatory intelligence and establishing strategy for submission of clinical trial applications (CTAs) and marketing authorisations (MAAs)Submission of regulatory files and responding to questions from health authoritiesEnsuring the preparation, review and submission of pre-meeting packages for health authority meetings as well...

About the RoleWe are seeking an experienced Regulatory Affairs Chemistry, Manufacturing and Control (RA CMC) Specialist to join our Synthetics & Cell Technologies Department in the RA CMC Biotech & Rare Disease area within Novo Nordisk.The successful candidate will provide strategic, tactical, and operational regulatory input to projects, leading activities...

Responsibilities:As a GCP Advisor Specialist, you will be responsible for managing updates to our standard operating procedures (SOPs) covering the Establish Clinical Evidence process, ensuring compliance with GCP and regulatory requirements.Your Key Responsibilities:Verify and approve Standard Operating Procedures (SOPs) and ensure compliance with external...

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...

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...

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...