Specialist in Medical Affairs

Job SummaryWe are seeking a highly motivated Regulatory Affairs Specialist to support our medical devices team.Main ResponsibilitiesAs a Regulatory Affairs Specialist, you will play a key role in ensuring compliance with regulatory requirements for our medical devices. Key responsibilities include preparing and submitting regulatory submissions to regulatory...

Regulatory Affairs Specialist Medical DevicesPage Personnel è alla ricerca di un Regulatory Affairs Specialist Medical Devices motivato e dettagliato per unirsi al nostro team. Il Regulatory Affairs Specialist Medical Devices svolgerà un ruolo chiave nell'assicurare la conformità con i requisiti regolatori per i dispositivi medici. Questo individuo...

Medical Manager - Anti-InfectivesAbout the Role: We are seeking a highly skilled Medical Manager to join our Medical Affairs team in Milan, Italy. As a Medical Manager, you will play a key role in managing medical projects, designing and implementing medical education and clinical trial projects, and collaborating with global colleagues and physicians.Key...

About the OpportunityWe are seeking a highly skilled Medical Affairs Manager to join our team in Milan, Italy. As a key member of our Medical Affairs team, you will be responsible for developing and implementing medical strategies to support the launch of our products in the region.Key Responsibilities• Develop and execute medical strategies to support...

About the RoleWe are seeking a highly motivated and detail-oriented Regulatory Affairs Specialist to support our client, a medical company that develops Class III, II, and I devices.Key ResponsibilitiesRegulatory SubmissionsPrepare and submit regulatory submissions to regulatory authorities, including 510(k) premarket notifications, Technical Files, Design...

Job DescriptionWe are seeking a highly motivated and detail-oriented Regulatory Affairs Specialist to support our medical device team.The successful candidate will play a key role in ensuring compliance with regulatory requirements for our medical devices.This individual will collaborate cross-functionally with internal teams to support product development,...

About the RoleWe are seeking a highly motivated and detail-oriented Regulatory Affairs Specialist to play a key role in ensuring compliance with regulatory requirements for our medical devices. In this position, you will collaborate with internal teams to support product development, registration, and post-market compliance activities.Key...

Job Title: Associate Director, Regulatory Affairs Medical Device Lifecycle ManagementJob Type: Full Time, Permanent PositionLocation: HybridRemuneration: Attractive salary and packageAbout the Role:We are seeking a highly experienced Associate Director, Regulatory Affairs Medical Device Lifecycle Management to join our team. As a key member of our Regulatory...

About the RoleWe are seeking a highly motivated and detail-oriented Regulatory Affairs Specialist to join our team at Page Personnel.

Job Title: Associate Director, Regulatory Affairs - Medical Device/Post Market SurveillanceJob Type: Full Time, Permanent PositionLocation: HybridRemuneration: Attractive salary and packageAn exciting opportunity to join a growing pharmaceutical company that specializes in Cancer and Supportive Care, Gastroenterology, and Hepatology. Due to increasing...

Job Title: Senior Medical Strategy Lead - OncologyJob Summary:Regeneron Pharmaceuticals, Inc is seeking a Senior Medical Strategy Lead - Oncology to lead our medical strategy and drive our success in Italy. As a key member of our Medical Affairs team, you will be responsible for developing and executing medical strategies that align with our business...

About the RoleThis is a remote opportunity to develop and maintain peer-to-peer relationships with key medical experts, supporting trial enrollment, program protocol training, and ensuring healthcare professionals have the latest information on clinical development programs.Key ResponsibilitiesDevelop and maintain collaborations with medical experts,...

Job Title: Associate Director, Regulatory Affairs - Medical Device/Post Market SurveillanceJob Type: Full Time, Permanent PositionLocation: HybridRemuneration: Attractive salary and packageCpl Healthcare is seeking an experienced Associate Director, Regulatory Affairs - Medical Device Lifecycle Management to join their team. This role offers a unique...

Medical Manager PositionAt Mundipharma, we are seeking a dedicated Medical Manager to lead our Anti-Infectives team. This permanent role is based in Milan, Italy, and is part of our Medical Affairs department.ResponsibilitiesDevelop and execute strategies for Anti-Infectives medical affairs initiatives.Collaborate with cross-functional teams to ensure...

Job Title: Medical Science LiaisonThis role is a unique opportunity to develop and maintain peer-to-peer relationships with key medical experts. As a remote employee, you will collaborate with physicians and other medical experts to support trial enrollment, provide protocol training guidelines and best practices, and ensure that healthcare professionals...

Medical Manager RoleMundipharma is seeking a skilled Medical Manager to join our Medical Affairs team in Milan, Italy. As a Medical Manager, you will be responsible for providing medical support to our commercial, market access, and regulatory teams, as well as developing and implementing medical education and training programs.Key Responsibilities•...

Job Title: Associate Director, Regulatory Affairs - Medical Device/ Post Market SurveillanceJob Type: Full Time, Permanent PositionLocation: HybridRemuneration: Attractive salary and packageCpl Healthcare is seeking an experienced Regulatory Affairs Director to join their team. The ideal candidate will have a sound understanding of new registrations and...

Job Title: Associate Director, Regulatory Affairs - Medical Device/Post Market SurveillanceAbout the Role:As a key member of our Regulatory Affairs team, you will be responsible for the strategic lifecycle management of our Medical Devices. This includes oversight of all activities required for the successful and smooth integration of new products following...

At Shockwave Medical, Inc., we're pioneering the development and commercialization of Intravascular Lithotripsy (IVL) to treat complex calcified cardiovascular disease. As a Field Clinical Specialist, you'll play a critical role in increasing the adoption of our IVL technology by supporting customers' education, disseminating clinical data, and implementing...

Job Title: Senior Regulatory Affairs ManagerJob Type: Full Time, Permanent PositionLocation: Italy (Milan) – HybridRemuneration: Attractive salary and packageCpl Healthcare is seeking a Senior Regulatory Affairs Manager to join our team. As a key member of our Regulatory Affairs department, you will be responsible for the strategic lifecycle management of...