Trabajo Regulatory Affairs

Pharmacovigilance Associate - Norwegian & Swedish Language - Homebased Full-time Department: ICSR Management We are PrimeVigilance (part of Ergomed Group), a specialised mid-size pharmacovigilance service provider established in 2008. We are proud to have achieved global organic growth year after ye...

We are looking for a RAQA Consultant ( Regulatory Affairs / Quality Assurance ) to join our Clinical and Regulatory Team. This is an amazing opportunity to work on regulatory and quality consulting projects. We have a great skill set in data monitoring, content writing and consulting for multiple do...

Description We are the makers of possible BD is one of the largest global medical technology companies in the world. Advancing the world of health is our Purpose, and it’s no small feat. It takes the imagination and passion of all of us from design and engineering to the manufacturing and marketing ...

PURPOSE OF THE ROLE The main purpose of this role is to plan, direct, coordinate and oversee quality aspects of activities and duties of Global (GRA) and Local Regulatory Affairs (LRA) teams. This includes also the management and the coordination of quality of regulatory affairs pertinent to third p...

Medical Information Associate- Italian language Full-time Department: Medical Information We are PrimeVigilance (part of Ergomed PLC), a specialised mid-size pharmacovigilance service provider initially established in 2008. We are proud to have achieved global organic growth year after year, with st...

Join Caidya as a Senior Study Start-Up Lead (Sr. SSUL). You'll focus on managing the submission of global applications for clinical trials. The ideal candidate will independently handle CORE study documents, understand regulatory submissions globally, and manage submission processes with ethics comm...

Mission • The Global Clinical Program Lead (GCPL) is a core member of the Global Project Team and is leading the Strategic Clinical Team within Global Clinical Development, working cross functionally with other R&D and non-R&D departments such as Regulatory and Patient Safety, Disease Biology, Globa...

Regulatory Affairs · Barcelona · Fully Remote CMC Expert (Biologics) Do you want to join us as CMC Expert and boost your skills in a Global technical environment? Are you willing to contribute, learn and develop? Do you want to apply your knowledge in health sciences and RA in a dynamic and internat...

By clicking the “Apply” button, I understand that my employment application process with Takeda will commence and that the information I provide in my application will be processed in line with Takeda’s Privacy Notice and Terms of Use . I further attest that all information I submit in my employment...

Description JOB FUNCTION : Primarily focused on providing technical support in activities related to the development and implementation of local Studies for the generation of data in epidemiology and Real World Evidence studies (RWE). Maintain knowledge in legislation and local regulation for doing ...

Técnico de Registros / Regulatory Affairs - León Este profesional tendrá como responsabilidad principal la gestión de la documentación necesaria para la consecución de los registros/autorizaciones de puesta en el mercado de los nuevos medicamentos de uso veterinarios así como la gestión y seguimient...

Description We are the makers of possible BD is one of the largest global medical technology companies in the world. Advancing the world of health is our Purpose, and it’s no small feat. It takes the imagination and passion of all of us from design and engineering to the manufacturing and marketing ...

Description As a Government & Institutional Relations Lead , will be part of Hitachi Energy business and reporting to the Group Senior Vice President, Global Head of Government & Institutional Relations, you are responsible to ensure compliance with external regulatory requirements and implementatio...

We're looking for Regulatory Affairs Specialist in Madrid Inizio Engage is looking for a Regulatory Affairs Specialist for an important and well known pharma company. Leader in develop, manufacture and marketing a wide range of generic and OTC products. The Regulatory Affairs Specialist that we're l...

Regulatory Affairs Associate page is loaded Regulatory Affairs Associate Apply locations Barcelona posted on Posted 23 Days Ago job requisition id JR009439 With a unique legacy in dermatology as well as decades of cutting-edge innovation, Galderma is the pure-play dermatology category leader, presen...