Global Clinical Operations Manager

About the RoleWe are seeking an experienced Senior Clinical Project Lead to join our dynamic global clinical development team at Novo Nordisk, where you will play a key role in advancing ambitious drug development trials within the area of Cardiovascular, Kidney and Alzheimer Diseases (CKAD).In this senior role, you will be accountable for end-to-end...

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...

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...

Key ResponsibilitiesThis exciting opportunity offers a chance to lead global cross-functional study teams, drive clinical trials successfully, and collaborate with Novo Nordisk affiliates globally to accomplish goals.You will assume accountability for end-to-end planning, execution, and completion of global trials. This includes leading the global...

Job DescriptionWe are seeking a highly experienced and skilled Global Clinical Development Leader to join our team at Novo Nordisk A/S.About the RoleIn this key position, you will be responsible for driving the planning and design of clinical studies and providing medical oversight during study conduct.You will work closely with cross-functional teams,...

Are you ready to join a dynamic global clinical development team at Novo Nordisk, where you'll play a key role in advancing ambitious drug development trials within the area of Cardiovascular, Kidney and Alzheimer Diseases (CKAD)? Would you like to be part of an innovative complex global trial portfolio, be part of a team with an innovative mindset and...

Are you ready to join a dynamic global clinical development team at Novo Nordisk, where you'll play a key role in advancing ambitious drug development trials within the area of Cardiovascular, Kidney and Alzheimer Diseases (CKAD)? Would you like to be part of an innovative complex global trial portfolio, be part of a team with an innovative mindset and...

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...

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...

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...

Novo Nordisk A/S is a leading global healthcare company with a 100-year legacy of driving change to defeat serious chronic diseases. As a Clinical Outcome Assessment Specialist, you will be part of this ambitious journey towards ensuring that patients' experiences, perspectives, needs, and priorities are captured and meaningfully incorporated into drug...

About the PositionWe are seeking a highly skilled and experienced Regulatory Document Specialist 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 oversight...

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...

Join us as a Principal Digital Process Lead, where you will leverage your expertise in GCP and regulatory requirements to drive digital transformation across our clinical process management team.Your key responsibilities will include:Digitalisation of key processes and proceduresVerifying and approving Standard Operating Procedures (SOPs) and ensuring...

Select how often (in days) to receive an alert: Create AlertClinical Outcome Assessment Specialist - Parental Leave CoverCategory: Clinical DevelopmentLocation:Søborg, Capital Region of Denmark, DKWould you like to be a part of the ambitious journey towards ensuring that patients' experiences, perspectives, needs, and priorities are captured and...

Jobbeskrivelse Placering Søborg, Denmark Jobkategori Procurement Ansøg nu Are you motivated by the opportunity of being part of an ambitious clinical outsourcing team? Do you understand the pharma business, have a strategic mind-set and strong communication skills as well as an interest in working with suppliers in the clinical drug development space?...

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...

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 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...

RQ&C OperationsThe RQ&C Digital Transformation department is responsible for driving change within the RQ&C organization to optimize and digitalize processes across the five areas: Regulatory Affairs, R&D Quality, Clinical Reporting, Digital Transformation, and Global Safety. As a Regulatory Data Partner, you will play a key role in implementing and...