Regulatory Affairs Director Jobs in Madrid

At Johnson & Johnsonwe believe health is everything. Our strength in healthcare innovation empowers us to build aworld where complex diseases are prevented treated and curedwhere treatments are smarter and less invasive andsolutions are our expertise in Innovative Medicine and MedTech we are uniquel...

Primary Function of Position:The Regulatory Affairs Specialist plays an important role within the Regulatory Affairs Department focusing on providing advanced regulatory support for New Product Development (NPD) market expansion and sustaining operations across designated Business Units. This positi...

The Specialist Study Start Up and Regulatory Affairs leads and coordinates all activities related to achieving site initiation readiness. The role provides subject matter expertise ensures regulatory compliance and serves as a key liaison between internal teams clients and external stakeholdersAccou...

Careers that change lives start here. Medtronic is a global leader in healthcare technology with a Mission to alleviate pain restore health and extend life. Our 95000 employees work across more than 150 countries to put patients first developing innovative medical technologies that improve the lives...

Position Purpose:This role is responsible for providing support to clients of Compliance Services. The Compliance Services team provide services to the pharmaceutical and med device industries. Work including Transparency Support and Outsourcing Grants Management HCP Screening and Tiering and HCP Co...

We anticipate the application window for this opening will close on - 9 Oct 2026Careers that change lives start here. Medtronic is a global leader in healthcare technology with a Mission to alleviate pain restore health and extend life. Our 95000 employees work across more than 150 countries to put...

IMPORTANT: after you apply please check your email. We send you a link to complete your application it is not considered until that last step is done. If you do not see it check your spam folder.This is a fully remote position open to candidates based in Spain.Pay: $50$80/hrRole Title: Regulatory Af...

The Specialist Study Start Up and Regulatory Affairs leads and coordinates all activities related to achieving site initiation readiness. The role provides subject matter expertise ensures regulatory compliance and serves as a key liaison between internal teams clients and external stakeholdersAccou...

Te gustaría desarrollarte en el área de Regulatory Affairs Calidad y Medio Ambiente dentro de una empresa consolidada en el sector sanitario Esta posición es para ti!Desde la división RAS RECRUITING especializada en selección directa te acompañamos en la búsqueda de tu nuevo proyecto profesional. Ac...

Position: Regulatory Affairs Associate - TemporaryLocation: MadridExperience: 3 years of experience in similar roles within the pharmaceutical sectorWant to know more Exeltis is part of Insud Pharma a global pharmaceutical group operating across the entire value chain with extensive expertise in sci...

The Senior Specialist Study Start Up and Regulatory Affairs leads and coordinates all activities related to achieving site initiation readiness. The role provides subject matter expertise ensures regulatory compliance and serves as a key liaison between internal teams clients and external stakeholde...

Revolution Medicines is a global commercial-state oncology company dedicated to discovering developing and delivering innovative medicines for patients with RAS-addicted cancers. Leveraging its differentiated RAS(ON) tri-complex inhibitor platform the company is advancing a broad integrated portfoli...

Revolution Medicines is a late-stage clinical oncology company developing novel targeted therapies for patients with RAS-addicted cancers. The companys R&D pipeline comprises RAS(ON) inhibitors designed to suppress diverse oncogenic variants of RAS proteins. The companys RAS(ON) inhibitors daraxonra...

Job OverviewIndividual contributor with advanced knowledge acquired from at least 8 years of relevant industry experience. Working independently with limited supervision the individual will provide strategic regulatory expertise and leadership for clinical trial applications and lifecycle management...

Our team members are at the heart of everything we do. At Cencora we are united in our responsibility to create healthier futures and every person here is essential to us being able to deliver on that purpose. If you want to make a difference at the center of health come join our innovative company...

Our team members are at the heart of everything we do. At Cencora we are united in our responsibility to create healthier futures and every person here is essential to us being able to deliver on that purpose. If you want to make a difference at the center of health come join our innovative company...