Global Medical Affairs Expert

We are seeking a Talent Partner for Global Medical Affairs to join our P&O Business Partnering unit in Development. As a key member of our leadership team, you will be responsible for driving organisational development and effectiveness, strategic workforce management, change management, culture, and engagement.You will work closely with business leaders and...

Radiobotics is a dynamic and innovative company dedicated to solving the global need for radiologists while ensuring every patient receives expert-level care. We are looking for a talented QA/RA specialist to join our Clinical and Regulatory team and contribute to our mission.The ideal candidate will have a strong background in quality assurance and...

In our line of work, life isn't a given - it's the ultimate goal. When life takes an unexpected turn, our technology and solutions enable caregivers to make informed diagnostic decisions to improve patient care. This is our shared purpose at Radiometer and what unites all +4000 of us - no matter our roles or where in the world we're located. Creating...

Job Description">Lundbeck A/S, H is seeking a Medical Affairs Team Lead - Clinical Operations to join our Medical Affairs team. As a key member of our team, you will be responsible for leading and managing clinical trials across various locations, working closely with colleagues from different departments and external partners.">About the Role">We are...

Welcome to Euro Federation of Organizations for Medical Physics - EFOMP, where we strive to bring innovative medical solutions to the market while prioritizing patient safety and well-being. As a Regulatory Affairs Manager, you will be a crucial member of our team, responsible for ensuring our products comply with relevant regulations and standards.You will...

About the Role:Pharma IT is seeking experienced Senior/Principal Medical Writer Consultants to join our Regulatory Affairs & Medical Writing Team. As a consultant, you will work with clients in the pharma, biotech, and medical device industries.Responsibilities:Write and review clinical documents for regulatory submissions in the EU and US.Participate in...

Job DescriptionMain Responsibilities:• Drive key internal and external medical and scientific activities to support our current portfolio and shape future development in acute care diagnostics.• Collaborate with cross-functional teams to develop strategic projects and commercial activities.• Establish relations with healthcare professionals and key...

Are you motivated to drive change and help improve the lives of people living with chronic diseases? Do you want to be part of a dedicated team with the aim of securing a leading position within the treatment of obesity, diabetes, and other cardiometabolic and renal diseases? Then apply today and join us as our new Regional Medical Advisor in Novo Nordisk...

We are seeking an experienced Medical Device Compliance Expert to join our team at Euro Federation of Organizations for Medical Physics - EFOMP.This is a unique opportunity to apply your knowledge of medical device regulations and standards to help shape our product development and commercialization strategies. As a key stakeholder, you will be responsible...

About the OpportunityWe are seeking a passionate Senior Manager/Associate Director (dependent on experience) to join our growing team in Global Medical Affairs. As a key member of our organization, you will play a crucial role in the development and execution of our external programs across the endocrine portfolio at an above-country level.Your primary...

Job DescriptionThe Regulatory Affairs team at Genmab A/S is seeking an experienced professional to fill the role of Director/Associate Director, Global Regulatory Affairs. The successful candidate will be responsible for providing strategic regulatory guidance on CMC topics, collaborating with cross-functional peers, and planning and preparing CMC...

**Job Description:**Your role as a Therapeutic Area Specialist with Merck Gruppe involves engaging in meaningful conversations with healthcare professionals about our Neurology & Immunology portfolio. You will lead customer interactions and coordinate with internal resources to enhance customer engagement, ensuring a seamless experience.This role requires...

Location: Denmark Overview: We are excited to announce a new opportunity for a Medical Science Liaison to join an expanding team. This role combines traditional field-based MSL activities with strategic Medical Advisor responsibilities, covering a range of therapy areas across the Nordics. Key Responsibilities: KOL Engagement: Identify, establish, and...

About This RoleThe Medical Advisor will be responsible for driving medical input to commercial activities, identification, and networking with key external experts, planning, and execution of advisory boards and cooperation with experts inside Radiometer on key strategic projects. As a Medical Advisor, you will have the opportunity to create an impact on our...

At Radiometer Danmark, we're committed to improving global healthcare with reliable, fast, and easy patient diagnoses. As a key member of our Global Regulatory Affairs team, you'll play a crucial role in driving process improvements and implementing systems and tools to support efficient regulatory support for the organization and growth of the company.Job...

We are Radiobotics, a company driven by aspiration, curiosity, and playfulness. We strive to learn what happens beyond the surface and show up every day ready to engage and have fun with each other. Our vision is to solve the global need for radiologists while ensuring every patient receives expert-level care.As a Quality Management System Professional, you...

The Director of Regulatory Affairs at Black Swans Exist is responsible for ensuring that the company's products meet global regulatory requirements, focusing on the USA and Europe. This role develops and executes regulatory compliance strategies, navigates approval processes for pharmaceuticals and medical devices, and ensures timely updates for existing...

The Director of Regulatory Affairs ensures that the company's products meet global regulatory requirements, focusing on the USA and Europe, including those set by the FDA, EMA, and other relevant authorities. This role is responsible for developing and executing regulatory compliance strategies, navigating approval processes for pharmaceuticals and medical...

Are you passionate about quality and regulatory affairs in the medical device industry? Do you have a strong background in quality management systems and regulatory requirements? We are seeking a talented QA/RA specialist to join our Clinical and Regulatory team at Radiobotics and contribute to our mission of solving the global need for radiologists while...

About the JobGenmab A/S is seeking an experienced Director/Associate Director, Global Regulatory Affairs to join our Regulatory Affairs team. The successful candidate will provide strategic regulatory guidance on CMC topics, collaborate with cross-functional peers, and plan and prepare CMC documentation for clinical applications, marketing authorization...