Clinical Affairs Director

Company OverviewNordberg Medical is a Swedish biotech company committed to innovation in biomaterial science. We aim to improve lives through the production and marketing of innovative medical products targeting structural imbalances associated with aging.Job DescriptionThis role will be pivotal in establishing strategic and tactical Medical Affairs...

A Company on the MoveNordberg Medical is revolutionizing biomaterial science to address functional loss. As a pioneer in this field, we've achieved significant milestones, including CE certification for our first product, JULÄINE of Sweden.This innovative biostimulator stimulates natural collagen production in the skin, opening doors to growth in the...

Regulatory Affairs Director Wanted!Haeger & Carlsson Executive Search & Interim AB is pleased to partner with a prominent life sciences company to find a highly skilled Regulatory Affairs Director. In this critical role, you will lead global regulatory strategies to support the submission and approval of biologics.The ideal candidate must have a strong...

TN Sweden, a dynamic medical device business, is seeking a Medical Affairs Manager to support their expansion in the Stockholm office.The successful candidate will provide medical and scientific support for the company's products, collaborating with management, regulatory affairs, and commercial teams to ensure product safety and effectiveness.This role...

Promote Ethical Business Practices in the Life Sciences IndustryTN Sweden seeks an experienced professional to serve as our Regulatory Affairs Director.In this key role, you will be responsible for developing and implementing comprehensive regulatory strategies to ensure compliance with European laws and regulations.Main Responsibilities:Cultivate strong...

About Nordberg MedicalNordberg Medical is a pioneering biotech company that leverages biomaterial science to restore functionality loss. Our cutting-edge biomaterials enable the development and marketing of innovative medical products addressing structural imbalances associated with aging.Our journey began with a critical milestone, receiving CE...

Transform Lives with Our Ventilation PlatformWe are seeking a clinical application specialist to join our product management team in Solna, Sweden. In this role, you will have the opportunity to develop new products and services that make a significant impact on patient care.Your primary responsibilities will include participating in the development of new...

Regulatory Affairs and Quality Expert - IMPWe are seeking a regulatory affairs and quality expert to join our team at Sobi. As a global company with over 1,800 employees in more than 30 countries, we are committed to an inclusive, sustainable and flexible workplace that fosters growth and development.Job Description:As the clinical quality assurance manager,...

At Velora Health AB - Stockholm, we're driven by a mission to democratize access to a healthy and long life through the fusion of precision medicine, technology, and a holistic approach to health.Our journey began with tackling one of the biggest global health issues – obesity, which affects 39% of the world's population. Through our digital health clinic...

Ventilation Platform Specialist NeededWe are seeking a ventilation platform specialist to join our product management team in Solna, Sweden. In this role, you will have the opportunity to develop new products and services that improve patient care.Your primary responsibilities will include participating in the development of new products and services,...

The regulatory affairs specialist will play a critical role in supporting the management of QMS processes in our virtual organisation. This includes managing, maintaining, and supporting the eQMS.Main Tasks & Responsibilities:Enter quality-related issues into the eQMS and track that actions and tasks are completed on time.Escalate any overdue records to the...

As a Medical Affairs Manager at TN Sweden, you will play a crucial role in supporting the company's growth and innovation in the medical device industry.Your primary responsibility will be to provide medical and scientific support for the company's products, ensuring that they meet regulatory requirements and effectively communicate their value to customers...

About Our RoleTaking on the position of Nordics Medical Affairs Lead at Seqirus, you will be responsible for collaborating with other regional health professionals to develop and execute strategies that improve public health in the Nordics region.With your advanced medical degree and extensive knowledge of product development and life cycle management, you...

We are looking for a Senior Legal Counsel to contribute to our purpose by providing strategic legal support in a dynamic organization. As a member of the Group Legal Affairs & Compliance team, you will be responsible for managing group-wide legal matters and supporting our central functions.Key responsibilities include corporate governance, managing legal...

TN Sweden is a pioneering medical device business dedicated to harnessing cutting-edge biotechnological manufacturing methods to drive innovation in biomaterials.As a Medical Affairs Manager, you will contribute to this mission by providing medical and scientific support for the company's products, collaborating with management, regulatory affairs, and...

Gilead Sciences, Inc. is a leader in the development of innovative treatments for patients with life-threatening diseases.Role OverviewThe Senior Medical Manager will play a critical role in evolving our culture and creating an environment where every employee feels included, developed, and empowered to fulfill their aspirations.Responsibilities...

At PharmaRelations ApS, we are committed to making brands more successful. To achieve this goal, we are seeking an experienced Senior Director to lead our regulatory affairs department in the Nordic region.Key ResponsibilitiesDeveloping and implementing regional regulatory strategies.Critical evaluation of submission packages.Mentoring and guiding the...

Responsibilities and RequirementsThe Clinical Affairs Specialist will be responsible for the following key areas:Protocol development and managementRegulatory submissions and documentationInvestigator communication and coordinationStudy timelines and budget managementRequirements for this role include:Life sciences degree or equivalent experienceExperience...

As a Field Enablement Director at BTR Group in Stockholm, you will be responsible for developing and implementing strategies to drive successful product launches and business processes.Key AccountabilitiesIdentify needs of independent centers regarding product launches and implementation of client products in their clinical routine.Drive initiatives to...

Immense Group is seeking an experienced Legal Operations Director to lead our Legal and Compliance department. The ideal candidate will have a strong track record of managing complex legal and regulatory affairs in the online gaming and betting industry.The successful candidate will be responsible for providing strategic leadership to the Legal and...