Clinical Outcome Assessment Specialist

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...

Would you like to be a part of the ambitious journey towards ensuring that patients' experiences, perspectives, needs, and priorities are captured and meaningfully incorporated into drug development and evaluation? Are you ready to shape the future of clinical trials through clinical outcomes assessment (COA)? Do you thrive in cross-functional collaborations...

At Novo Nordisk, we are committed to creating innovative treatments for people living with serious chronic diseases. Our ambition is to ensure that patients' experiences, perspectives, needs, and priorities are captured and meaningfully incorporated into drug development and evaluation.We are seeking a Clinical Outcome Assessment Specialist who will play a...

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...

We are passionate about connecting the Medical & Science organization while driving scientifically sound medical deliverables across the Novo Nordisk project portfolio. 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...

We are committed to driving scientifically sound medical deliverables across our project portfolio at Novo Nordisk. To achieve this goal, we need a skilled Clinical Outcome Assessment Specialist who can develop COA strategies, interact with health authorities, and select, modify, develop, validate, and implement fit-for-purpose COAs in clinical trials.The...

Novo Nordisk is a leading global healthcare company dedicated to defeating serious chronic diseases. We recognize the importance of capturing patients' experiences, perspectives, needs, and priorities in our drug development and evaluation processes.We are looking for a Clinical Outcome Assessment Specialist who will drive the development of COA strategies,...

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...

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 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...

Clinical Outsourcing Management OverviewClinical Outsourcing Management is a key component of Novo Nordisk's Global Trial Portfolio, responsible for managing the clinical contracting process from request for information to signed contract. This involves close collaboration with internal and external stakeholders to drive and execute clinical trials...

Key ResponsibilitiesAs a Contract Management Specialist, 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 collaboration and successful project outcomes.The ideal candidate will have a strong understanding of...

Novo Nordisk A/S is a leader in the global healthcare industry with a rich history of innovation and commitment to improving patient lives. As a Clinical Outcome Assessment Specialist, you will have the opportunity to make a meaningful impact in the development of new treatments for patients living with serious chronic diseases.This role is a one-year...

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...

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 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...

Are you an experienced Medical Writer looking to grow your career? If yes, then we would love to hear from you.The positionAs Medical Writing Specialist, your main responsibility is to drive the preparation of complex clinical documents and act as project manager. More specifically, you are expected to lead tasks such as:Planning, development and oversight...

We are seeking a Senior Clinical Leader to join our team and lead the medical strategy for our MASH and liver diseases portfolio. As a key member of our global medical affairs team, you will play a critical role in shaping the future of our company's medical strategy.Your expertise will be essential in leading strategic discussions, developing medical plans,...

About the Job:The GMP Raw Materials Specialist will be responsible for ensuring regulatory compliance, assessing vendor change notifications, and providing strategic input on raw material-related matters. This role requires collaborating with Supplier Qualification Management, Procurement, QA, and Process Teams to assess material and supplier risks. You will...

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...