Medical Lead

Select how often (in days) to receive an alert: Beyond the skin The Thrombosis Business Unit in LEO Pharma is uniquely positioned to make a significant difference for patients. We focus on high-risk patient groups and supporting healthcare systems with high quality medicines. With 80 years' experience, we empower healthcare professionals with expert...

The role of Medical Documentation Lead at Lundbeck A/S, H is a pivotal one. As the Head of Regulatory Content, you will lead and manage the Medical Documentation department. This involves driving the digital transformation and enhancing R&D productivity through change management initiatives, implementation of innovative digital platforms, and upskilling team...

At LEO Pharma, we are dedicated to making a significant difference in the lives of patients with blood clots and other critical-care conditions.About the RoleThe Global Medical Lead will be responsible for leading the global medical strategy and setting impactful results-driven strategic direction for the global and country teams.Key ResponsibilitiesOverall...

LEO Pharma's Thrombosis Business Unit is a unique entity poised to make a significant difference for patients. We focus on high-risk patient groups and support healthcare systems with high-quality medicines.We empower healthcare professionals with expert treatments for illnesses involving blood clots and other critical-care conditions.The unit shares a...

LEO Pharma is committed to making a difference in the lives of patients with blood clots and other critical-care conditions.About the OpportunityThe Medical Lead will play a critical role in driving business growth and improving patient outcomes through the development and execution of a global medical strategy.Key AccountabilitiesDevelop and implement a...

About the CompanyNovartis is a leading global pharmaceutical company committed to discovering innovative solutions to address some of the world's most pressing health challenges.Your Role in the CompanyAs a Medical Lead at Novartis, you will be responsible for ensuring medical enquiries are responded to in a high-quality, timely manner and in accordance with...

As a member of the Thrombosis Business Unit, you will have the opportunity to make a significant impact in the lives of patients with blood clots and other critical-care conditions.About the PositionThe Medical Lead will be responsible for leading the global medical strategy and setting impactful results-driven strategic direction for the global and country...

At LEO Pharma, we're dedicated to empowering healthcare professionals with expert treatments for illnesses involving blood clots and other critical-care conditions.We're seeking a skilled Medical Advisor to join our global medical affairs team, working closely with local medical affairs teams, global medical information, and global market access.This role...

Job OverviewKite, a Gilead company, is seeking a Senior Medical Manager to cover Denmark. This role will be key in leading Medical Affairs initiatives and providing medical support to cross-functional teams within cell therapy.About UsGilead Sciences, Inc. is a research-based biopharmaceutical company that discovers, develops, and commercializes innovative...

As a Senior Engineer at Pharmalogic, you will work on-site at our clients' facilities, focusing on medical device manufacturing tasks or activities under the Medical Device QMS.You will be responsible for change requests, risk analysis/mitigation, quality assurance, SOP updates, and deviation handling.Required Skills and QualificationsDeep experience in...

Job OverviewWe are seeking a highly motivated and experienced professional to fill the role of Senior Manager/Associate Director, External Programs. As a key member of the Ascendis Pharma team, you will play a crucial role in the development and execution of external programs across the endocrine portfolio at an above-country level. This includes overseeing...

We are seeking an experienced regulatory affairs expert to join our Clinical and Regulatory team at Radiobotics. As a key member of our team, you will play a crucial role in ensuring our medical devices comply with international regulations and standards.In this role, you will collaborate closely with the development team to co-drive product release projects...

We are seeking a highly skilled Medical Device QA/RA specialist to join our Clinical and Regulatory team at Radiobotics. This is an exciting opportunity for someone with experience in quality assurance and regulatory affairs, who is passionate about ensuring the highest standards of product quality.Company OverviewRadiobotics is a leading company in the...

About the Opportunity:Join our dynamic team as a Medical Information Specialist and contribute to our mission of improving healthcare outcomes through high-quality, affordable medicines. In this role, you will have the opportunity to work collaboratively with cross-functional teams to deliver medical information services that meet the needs of healthcare...

About the RoleWe are seeking a highly skilled and experienced Senior Design Control Specialist to join our Device Development team. The successful candidate will play a crucial role in the development of new drug delivery solutions and will work closely with cross-functional teams to achieve extraordinary results.The ideal candidate will have a relevant...

Job Description:We are looking for a Regulatory Affairs Expert for Medical Devices to join our Clinical and Regulatory team. The ideal candidate will have a strong background in regulatory affairs, with experience in medical devices. You will be responsible for ensuring that our medical devices meet the highest regulatory standards and that we comply with...

Senior Director, Head of Medical Documentation Requisition ID: 5988 Location: Copenhagen, Danish Capital Region, DK Senior Director, Head of Medical Documentation Join Lundbeck as the Head of Medical Documentation and play a pivotal role in shaping our commitment to advancing brain health. This position offers a unique opportunity to create a lasting impact...

Your Role: As a Medical Writing and Clinical Disclosure Professional, you will play a crucial part in planning, managing, and writing clear, concise, and audience-friendly regulatory, scientific, and medical documents. Your main tasks will include:Writing and editing original regulatory, scientific, and medical documents at a professional level.Leading and...

About the Role:This is an exciting opportunity to join our team as a Medical Device Quality Assurance Specialist. As a key member of our Clinical and Regulatory team, you will be responsible for ensuring that our medical devices meet the highest quality standards. Your expertise in quality assurance and regulatory affairs will play a crucial role in driving...

Company Overview:Sandoz International GmbH is a leading global pharmaceutical company dedicated to improving healthcare outcomes through high-quality, affordable medicines. Our mission is to empower patients and healthcare professionals with the latest medical information and innovative solutions.Job Description:We are seeking an experienced Medical...