Quality Assurance Expert for Clinical Trials

About the RoleIn this exciting position, you will have the opportunity to make a difference in the lives of people participating in clinical trials by ensuring safe and high-quality products manufactured in compliance with legislation. Your key responsibilities will include ensuring best-in-class quality assurance of API for clinical trials in phase I, II,...

Job Overview">We are seeking a highly motivated and experienced Quality Assurance Professional to join our CMC API QA team. The successful candidate will support CMC API Development within the raw material and CMO shipping area, ensuring compliance with regulatory requirements, quality standards, and company policies.This role is part of our development...

Job OverviewWe are seeking a highly motivated and experienced Senior Quality Assurance Professional to join our CMC API QA team. As a Senior QP delegate, you will play a crucial role in ensuring the quality and safety of products for clinical trials and securing the development pipeline in Novo Nordisk.The successful candidate will be responsible for...

Clinical Trial Submission RoleWe are looking for an accomplished Clinical Trial Submission Manager to lead the submission of initial Clinical Trial Applications (CTAs) and amendments to Health Authorities (HAs) and Ethics Committees (ECs). As part of our dynamic CTA Management department, you will work closely with various stakeholders across Development and...

About Clinical Outsourcing ManagementClinical Outsourcing Management plays a vital role in supporting Novo Nordisk's Global Trial Portfolio projects. Our team works closely with internal and external stakeholders to drive and execute clinical trials worldwide. We are responsible for managing the clinical contracting process from request for information to...

Job DescriptionAs a Senior Clinical Project Lead, you will be responsible for end-to-end planning, execution, and completion of global trials. Your main responsibilities will include leading global cross-functional study teams, ensuring the trial team is well-functioning and effective, chairing of the trial squad, being overall accountable for the studies...

OverviewAt Novo Nordisk A/S, we are committed to advancing ambitious drug development trials within established and new therapeutic areas. As a Senior Clinical Project Lead, you will play a key role in driving successful delivery of our clinical trials and contributing to our mission to make a meaningful difference in the lives of people affected by serious...

About the PositionNovo Nordisk A/S is seeking an experienced Clinical Development Expert to drive the preparation of complex clinical documents and act as a project manager. As a key member of our Clinical Reporting team, you will play a crucial role in communicating scientific information to diverse stakeholders.The position requires a high level of...

About the JobWe are looking for a highly skilled and experienced Clinical Project Manager Medical Writing to join our team in Clinical Reporting. As a key member of our function, you will be responsible for driving the preparation of complex clinical documents and acting as project manager.Main ResponsibilitiesLead tasks such as planning, development, and...

Job DescriptionWe are looking for a highly motivated and experienced Quality Assurance Professional to join our CMC API QA team. As a member of our team, you will support CMC API Development within the raw material and CMO shipping area, ensuring compliance with regulatory requirements, quality standards, and company policies.Your key responsibilities will...

Clinical Trial Submission Job DescriptionThis is a unique opportunity to join our CTA Management department as a Clinical Trial Submission Manager. In this role, you will lead the submission of initial Clinical Trial Applications (CTAs) and amendments to Health Authorities (HAs) and Ethics Committees (ECs). You will collaborate closely with stakeholders...

About Novo NordiskNovo Nordisk A/S is a dynamic company that drives innovation in the pharmaceutical industry. We are dedicated to developing and delivering life-changing treatments for patients worldwide.We are seeking an experienced Clinical Trial Submission Manager to join our team, where you will be responsible for leading the submission of initial...

About This RoleWe are seeking an experienced Clinical Trial Submission Manager to join our CTA Management department. As a key member of our team, you will be responsible for leading the submission of initial Clinical Trial Applications (CTAs) and amendments to Health Authorities (HAs) and Ethics Committees (ECs). You will collaborate closely with...

About the RoleWe are seeking a highly skilled and experienced QA Specialist to join our team in Clinical Trials. As a member of our Quality Assurance department, you will play a crucial role in ensuring the quality and safety of products for clinical trials. In this dynamic environment, you will work closely with our team of experts to deliver best-in-class...

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...

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

About the RoleWe are seeking an experienced Clinical Outsourcing Expert to support our Global Trial Portfolio projects. As an integral part of our team, you will be responsible for managing clinical contracting processes from request for information to signed contract. You will work closely with internal and external stakeholders to ensure seamless...

About the RoleAt Novo Nordisk A/S, we are seeking a skilled and motivated Quality Assurance Expert to join our team. In this role, you will play a crucial part in ensuring patient safety by delivering high-quality standards for our products and production processes.The PositionAs an Aseptic Manufacturing Specialist, your primary task will be to review and...

About the PositionWe are seeking a highly skilled QA Specialist to join our team in Bagsværd, Denmark. As a QA Specialist, you will play a crucial role in ensuring the quality and safety of products for clinical trials.The successful candidate will be responsible for setting the quality direction for the capacity expansion project, delivering best-in-class...

RequirementsWe are looking for a highly motivated and experienced individual to join our team as a Senior Clinical Project Lead. The ideal candidate will have a strong background in clinical operations and a proven track record of delivering successful projects.You will be responsible for leading cross-functional study teams, driving clinical trials...