Global Regulatory Affairs Manager – Veterinary

Buscamos un Gerente de Asuntos Regulatorios para dirigir la estrategia regulatoria en España y Europa. Gestionará expedientes, coordinará departamentos e interactuará con autoridades como AEMPS y EMA, asegurando el cumplimiento del producto.

Worldwide Clinical Trials is a global CRO seeking a senior Regulatory Affairs professional to lead regulatory submissions across EMEA, Asia Pacific, and Latin America, ensuring ongoing compliance with evolving regulations and key regulatory documents. You will coordinate ethics submissions, provide strategic regulatory guidance, and mentor junior staff while...

Worldwide Clinical Trials is a global CRO seeking a senior Regulatory Affairs professional to lead regulatory submissions across EMEA, Asia Pacific, and Latin America, ensuring ongoing compliance with evolving regulations and key regulatory documents. You will coordinate ethics submissions, provide strategic regulatory guidance, and mentor junior staff while...

Company Description Medicine moves forward here. So will you. Ergomed is a specialist clinical research organization focused on rare disease and select oncology indications. We focus on the most complex trials, the studies where experience, judgement, and rigorous operational accountability make the biggest difference. We partner with small to midsize...

Position: Regulatory Affairs Biosimilar Specialist LATAM Location: Madrid Experience: 5+ years in Regulatory Affairs within innovative biopharmaceuticals and/or biosimilars Want to know more? At Exeltis, we continue to grow and we are looking for a Regulatory Affairs Biosimilar Specialist ready to take the next step in their career in an international,...

LocationsMadrid, SpainBelgrade, SerbiaLisbon, PortugalBudapest, HungaryAthens, GreeceBarcelona, SpainSofia, BulgariaBucuresti, RomaniaContract TypeFull timeJob OverviewIndividual contributor with advanced knowledge acquired from at least 8 years of relevant industry experience. Working independently with limited supervision, the individual will provide...

Regulatory Affairs Specialist, EMEAWork mode: Hybrid Onsite Location(s): Madrid, M, ES Location: in our offices in Madrid, Spain, on a hybrid working schedule (3 days per week in the office 2 days per week working from home). About the role:The Clinical Center of Excellence (CoE) is part of the EMEA Regulatory Affairs team and provides regulatory expertise...

Job Overview Individual 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 activities, with a strong focus on EU Clinical Trials...

Regulatory Affairs Specialist, EMEA Work mode: Hybrid Onsite Location(s): Madrid, M, ES Location: in our offices in Madrid, Spain, on a hybrid working schedule (3 days per week in the office 2 days per week working from home). About the role: The Clinical Center of Excellence (CoE) is part of the EMEA Regulatory Affairs team and provides regulatory expertise...