Regulatory Affairs Associate

Regulatory Affairs Associate, Health City: Soborg We are Reckitt Home to the world's best loved and trusted hygiene, health, and nutrition brands. Our purpose defines why we exist: to protect, heal and nurture in the relentless pursuit of a cleaner, healthier world. We are a global team united by this purpose.Join us in our fight to make access to the...

Regulatory Affairs Associate, Hygiene City: Soborg We are Reckitt Home to the world's best loved and trusted hygiene, health, and nutrition brands. Our purpose defines why we exist: to protect, heal and nurture in the relentless pursuit of a cleaner, healthier world. We are a global team united by this purpose.Join us in our fight to make access to the...

Do you want to work globally in an innovative company making products available for patients worldwide? We offer you an exciting and challenging position in an entrepreneurial and international company, with a short line of command. As our new Associate Director, you will be responsible for activities that are central to Ascendis Pharma’s global strategy,...

Regulatory Affairs Specialist, IVDR Agilent inspires and supports discoveries that advance the quality of life. We provide life science, diagnostic and applied market laboratories worldwide with instruments, services, consumables, applications, and expertise. Agilent enables customers to gain the answers and insights they seek -- so they can do what they do...

About the RoleWe are seeking a skilled Regulatory Affairs Specialist to join our team at Novo Nordisk A/S. As a key member of our RA CMC Synthetics & Cell Technologies department, you will play a crucial role in driving regulatory affairs strategies and submission activities related to synthetic small molecule projects.ResponsibilitiesProvide strategic,...

Har du styr på fødevare-, foder- og kemilovgivningen? Har du gode kommunikative evner og formår at oversætte kompliceret lovstof til et sprog andre forstår? Og brænder du for at tegne vores regulatoriske område, sætte din faglighed i spil og gøre en forskel i en succesfuld virksomhed i vækst? Så er jobbet som Regulatory Affairs Specialist hos os...

Job DescriptionWe are seeking an experienced Regulatory Affairs Specialist to join our team at Novo Nordisk A/S. As a CMC Regulatory Specialist, you will play a critical role in providing strategic, tactical, and operational regulatory input to projects.About the RoleIn this position, you will lead activities for synthetic small molecule projects in late...

Select how often (in days) to receive an alert: Create Alert Category: Reg Affairs & Safety Pharmacovigilance Location: Søborg, Capital Region of Denmark, DK We are expanding our product and project pipeline in Novo Nordisk and are looking for an engaged Regulatory Affairs Chemistry, Manufacturing and Control (RA CMC) Specialist with expertise in synthetic...

At Reckitt Benckiser, we protect, heal, and nurture in the relentless pursuit of a cleaner, healthier world. Our purpose defines why we exist: to make access to the highest quality hygiene, wellness, and nourishment a right and not a privilege.About the RoleThis Regulatory Affairs Associate position is part of our dynamic Hygiene team. As a key member,...

Job OverviewAs a key member of our team, you will play a crucial role in shaping Merck's relationships with government entities and managing public policy matters and communication in Denmark.Salary: Estimated salary range is between 110,000 - 140,000 DKK per annum, depending on experience and qualifications.Job DescriptionWe are seeking a highly experienced...

Are you a strategic communicator motivated by change and relationship-building in a global environment? As Governmental Public Affairs & Communications Head at Merck, you will be responsible for securing and sustaining optimal strategic engagement plans and building coalitions with external stakeholders. With direct report to the General Manager, you...

We are looking for a highly motivated and experienced process optimization lead to join our regulatory affairs team at Novo Nordisk A/S. As a key member of our team, you will be responsible for driving process excellence, innovation, and digital transformation in a regulated global environment.The ideal candidate will have a strong background in life...

We are seeking a highly skilled Patient-Centric Drug Development Specialist to join our team at Novo Nordisk A/S. This is an excellent opportunity to contribute to the development of innovative treatments for patients with serious chronic diseases.About the RoleIn this role, you will play a pivotal part in developing and implementing clinical outcome...

Select how often (in days) to receive an alert: Create Alert Category: Reg Affairs & Safety Pharmacovigilance Location: Søborg, Capital Region of Denmark, DK Do you get energy from driving the optimisation and digitalisation of processes that contribute to bringing better medicines to patients as well as making your colleagues' work easier and more...

We are seeking an experienced Clinical Development Lead to join our team in Söborg, Denmark.As a Clinical Development Lead in Obesity Medicine, you will play a key role in driving the planning and design of clinical studies and providing medical oversight during study conduct.You will work closely with cross-functional teams, including trial management,...

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...

Obesity Clinical Development LeadThis is an exciting opportunity for a seasoned medical professional to join our team as a Clinical Development Lead in the Obesity area. As a key member of our Medical & Science department, you will be responsible for driving the planning and execution of global clinical studies and providing medical oversight during study...

Job SummaryWe are seeking a highly skilled and experienced Senior Clinical Document Specialist to join our team at Novo Nordisk A/S. As a key member of the Clinical Reporting department, you will be responsible for driving the preparation of complex clinical documents and acting as project manager.About the RoleIn this role, you will lead tasks such as...

Global Medical Director External Programs ASCENDIS PHARMA A/S Are you passionate about changing the lives of people living with rare diseases? Do you have experience leading the development and execution of Global Medical Affairs external programs? If so, now is your chance to join Ascendis Pharma as our new Global Medical Director External Programs. ...

Are you an experienced Medical Writer looking to grow your career? If yes, then we would love to hear from you. The position As 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...