Regulatory Affairs Associate Manager

Innovative solutions for a better tomorrowRadiometer Danmark / Danaher is committed to improving global healthcare with reliable, fast, and easy patient diagnoses. We strive to make a difference in people's lives by providing cutting-edge technology and solutions.The Senior Manager, RA Processes, Systems and Tools plays a crucial role in driving process...

Company OverviewRadiometer Danmark / Danaher is a leading company in the diagnostics industry, working towards improving global healthcare with reliable, fast, and easy patient diagnoses. We are proud to work alongside a community of six fellow Diagnostics Companies at Danaher.Job DescriptionThe Senior Manager, RA Processes, Systems and Tools for Radiometer...

About the PositionWe are seeking a highly skilled Regulatory Affairs professional to join our team as an Associate Director, Global Regulatory Affairs Project Lead. In this role, you will have the opportunity to utilize your expertise to drive regulatory compliance and quality in clinical trials.ResponsibilitiesDrive regulatory compliance and quality in...

Sandoz International GmbH is a leading generic and biosimilar medicines company, committed to improving access to high-quality, low-cost medicines for patients worldwide. We are seeking a highly motivated Global Regulatory Affairs Manager to join our LCM Product team.In this role, you will be responsible for managing global regulatory affairs, including...

We're dedicated to creating life-changing treatments at Genmab, and we're seeking a highly skilled Biopharmaceuticals Regulatory Affairs Specialist to join our Regulatory Affairs CMC team.Director/Associate Director, Global Regulatory Affairs - CMCIn this critical role, you will be responsible for providing regulatory CMC input to support worldwide...

About the RoleAs an Associate Director, Global Regulatory Affairs Project Lead at Genmab, you will play a key role in our Global Regulatory Affairs organization. Your primary responsibility will be to represent RA in the Clinical Trial Teams and ensure regulatory oversight and progress of multiple, often highly complex, clinical trial submission...

Regulatory Affairs - National & EU procedures Hurecon Copenhagen, Capital Region of Denmark, Denmark REGULATORY AFFAIRS – EU PROCEDURES - NORDIC LANGUAGE - REMOTE POSSIBLE DO YOU WANT: To use either your Danish, Swedish or Norwegian Language - together with your English language skills? To have the ability to work remote as your other colleagues within...

The Genmab Vacancy Website is hosted by our Global HR System vendor, Workday. If you have any questions related to the hosting of this site please contact us at Workday@Genmab.com.Director/Associate Director, Global Regulatory Affairs - CMCAt Genmab, we're committed to building extraordinary futures together, by developing antibody products and pioneering...

About the RoleWe are seeking a highly skilled Associate Director, Global Regulatory Affairs Project Lead to join our team at Genmab. This individual will be responsible for representing RA in the Clinical Trial Teams and ensuring regulatory oversight and progress of multiple clinical trial submission activities.The successful candidate will work closely with...

We are looking for a new colleague to join our Regulatory department. Oresund Pharma is seeking a dedicated and experienced Regulatory Affairs Manager; in this role you will be responsible for Oresund Pharma's products worldwide with the purpose to develop and maintain a product portfolio following regulatory requirements and commercial demands. As a...

Genmab is an international biotechnology company dedicated to improving the lives of patients through innovative and differentiated antibody therapeutics. Our team has invented next-generation antibody technology platforms and leveraged translational research and data sciences to create a proprietary pipeline including bispecific T-cell engagers,...

About the RoleThe Regulatory Affairs CMC team at Genmab is seeking a highly experienced Director/Associate Director to support worldwide development and commercialization of biological products.As a key member of the team, you will be responsible for developing and executing sound global regulatory CMC strategies for early and late-stage development, as well...

At Genmab, we're driven to push the boundaries of innovation in developing groundbreaking cancer treatments and therapies.Director/Associate Director, Global Regulatory Affairs - CMCWe're seeking a seasoned Regulatory Affairs Director Lead to join our team and play a pivotal role in shaping the future of biologics development. As a key member of our CMC...

We are looking for an exceptional Global Regulatory Affairs Manager to join our team. This individual will be responsible for developing and executing the EU/ROW regulatory strategy for assigned projects, representing RA in the Clinical Trial Teams, and ensuring progress of multiple clinical trial submission activities.The Role & DepartmentThis position...

Our CultureGenmab fosters a culture of collaboration, mutual respect, and open communication. Our team is composed of talented individuals who share a passion for innovation and excellence. We strive to create an environment where every employee feels valued, supported, and empowered to contribute to our shared success.About the PositionWe're seeking a...

At Genmab, we're committed to building extraordinary futures together, by developing innovative antibody products that change the lives of patients and the future of cancer treatment.The Regulatory Affairs CMC team is evolving and we are therefore looking for a Director/Associate Director to join our dynamic team. The successful candidate will be responsible...

About the RoleWe are seeking an experienced leader to join our Global Regulatory Affairs organization as a Senior Director, Regulatory Affairs Strategy-EU/RoW. This role will be responsible for developing global strategies to advance Genmab's portfolio of development pipeline candidate drugs and marketed products.The ideal candidate will have a strong...

About the RoleGenmab is seeking an experienced Senior Manager/Associate Director to lead our Global Regulatory Affairs organization as EU/ROW Regulatory Lead. In this role, you will represent RA in Clinical Trial Teams and work closely with CROs and internal stakeholders to ensure regulatory oversight and progress of clinical trial submissions in EU/ROW.Key...

At Genmab, we're committed to building extraordinary futures together, by developing antibody products and pioneering therapies that change the lives of patients and the future of cancer treatment and serious diseases. Our people are caring, candid, and impact-driven, and our business is innovative and rooted in science. We believe that being proudly unique,...

Job Title: Regulatory Affairs CoordinatorIQVIA Argentina is seeking a highly skilled Regulatory Affairs Coordinator to join our team. The successful candidate will be responsible for ensuring compliance with regulatory requirements, providing training and support to sites, and collaborating with the study team to track the progress of assigned studies.Key...