Empleos actuales relacionados con Senior Regulatory Affairs Consultant - Madrid - Parexel
-
Regulatory Affairs Manager
hace 1 semana
Madrid, España Cpl Life Sciences A tiempo completoDirect message the job poster from Cpl Life SciencesManaging Consultant - Regulatory Affairs & Quality @ Cpl Life Sciencesob Title: European Regulatory Affairs ManagerLocation: Madrid, Spain, HybridRemuneration: Competitive salary and packageRegulatory Affairs Manager opportunity working for an established pharmaceutical company that specialises in generic,...
-
Regulatory Affairs Manager
hace 4 días
Madrid, España Cpl Life Sciences A tiempo completoDirect message the job poster from Cpl Life SciencesPara una comprensión completa de esta oportunidad y de lo que se requerirá para ser un candidato exitoso, siga leyendo.Managing Consultant - Regulatory Affairs & Quality @ Cpl Life Sciencesob Title:European Regulatory Affairs ManagerLocation:Madrid, Spain, HybridRemuneration:Competitive salary and...
-
Regulatory Affairs Manager
hace 2 semanas
Madrid, España Cpl Life Sciences A tiempo completoob Title:European Regulatory Affairs Manager Location:Madrid, Spain, Hybrid Regulatory Affairs Manager opportunity working for an established pharmaceutical company that specialises in generic, OTC, and prescription medicines. The business is increasingly growing and is looking for a personable and detail-oriented professional to join the small team and lead...
-
Regulatory Affairs Manager
hace 2 semanas
Madrid, España Cpl Life Sciences A tiempo completoob Title: European Regulatory Affairs ManagerLocation: Madrid, Spain, HybridRegulatory Affairs Manager opportunity working for an established pharmaceutical company that specialises in generic, OTC, and prescription medicines. The business is increasingly growing and is looking for a personable and detail-oriented professional to join the small team and lead...
-
Regulatory Affairs Manager
hace 2 semanas
Madrid, España Cpl Life Sciences A tiempo completoob Title: European Regulatory Affairs ManagerRecuerde revisar su CV antes de enviar la solicitud. Además, asegúrese de leer todos los requisitos relacionados con este puesto.Location: Madrid, Spain, HybridRegulatory Affairs Manager opportunity working for an established pharmaceutical company that specialises in generic, OTC, and prescription medicines....
-
Senior Regulatory Affairs Specialist
hace 2 semanas
Madrid, España Indero A tiempo completoThe Senior Regulatory Affairs Specialist will provide leadership for assigned projects regarding all regulatory activities that lead to startup of clinical trials and will oversee global/multinational complex large clinical trial submissions. This role will be responsible for sponsor-facing regulatory leadership and management of regulatory deliverables...
-
Senior Global CMC Regulatory Affairs Manager
hace 3 días
madrid, España Oxford Global Resources A tiempo completoA leading consulting firm is seeking a Global CMC Regulatory Affairs Manager Consultant to support a top pharma company in Barcelona. This role involves providing regulatory insight, ensuring compliance with global regulations, and collaborating with various teams. Candidates must have a Bachelor's degree in Life Sciences, at least 5 years of experience in...
-
Senior Manager
hace 2 semanas
Madrid, España Cpl Life Sciences A tiempo completoob Title :European Regulatory Affairs ManagerLocation :Madrid, Spain, HybridRegulatory Affairs Manager opportunity working for an established pharmaceutical company that specialises in generic, OTC, and prescription medicines. The business is increasingly growing and is looking for a personable and detail-oriented professional to join the small team and lead...
-
Senior Regulatory Affairs Specialist
hace 6 días
Madrid, Madrid, España Indero (formerly Innovaderm) A tiempo completoThe Senior Regulatory Affairs Specialist will provide leadership for assigned projects regarding all regulatory activities that lead to startup of clinical trials and will oversee global/multinational complex large clinical trial submissions.This role will be responsible for sponsor-facing regulatory leadership and management of regulatory deliverables...
-
Técnico/a Regulatory Affairs
hace 3 semanas
Madrid, España AC Marca A tiempo completo¡En AC Marca seguimos creciendo!Estamos buscando un/a Técnico/a Senior de Regulatory Affairs para que se una al equipo de nuestra planta en Sant Llorenç d'Hortons.Si tienes al menos 5 años de experiencia como Técnico/a de Regulatory, idealmente especializados en diferentes categorías de producto como biocidas y producto sanitario, inglés alto y...
Senior Regulatory Affairs Consultant
hace 3 semanas
Overview We are seeking an experienced Regulatory Affairs professional to join our team as a European Labelling & Promotional Regulatory Specialist. This key position provides expert guidance across a Therapeutic business unit, delivering both strategic and operational regulatory input to cross-functional teams. The role can be home or office based in various European locations. Key Responsibilities EU Product Information Management : Create, update and maintain EU Product Information in line with CCDS, Agency RTQ, and current labelling requirements Serve as the key point of contact for EU Product Information for both internal and external stakeholders Lead reviews, round tables, and approvals for EU Product Information in appropriate systems according to SOPs Deliver competitive labelling searches and contribute to TCLP for early development assets Operational Excellence : Ensure timely tracking and management of all EU Product Information in appropriate systems Lead Readability Testing processes including vendor selection, agreement management, questionnaire review, and submission of final reports Coordinate Linguistic Review processes with LR Coordinator according to SOPs Communicate proactively with SPA for artwork and mock-up changes, participating in Change Control Processes Leadership & Collaboration : Lead the Local Labelling Committee for creation, review and approval of EU Product Information Serve on the EU Clearance Committee as primary regulatory reviewer for promotional materials Build strong relationships with EU and Global Regulatory teams, local business partners, SPA, and PLG teams Monitor changes in EMA labelling requirements and keep the organization informed of technology requirements Qualifications University degree in a life science discipline Strong knowledge of EU regulatory requirements for product labelling and promotional materials Experience with electronic content management systems and regulatory SOPs Excellent project management and organizational abilities Outstanding written and verbal communication skills Proven ability to work effectively in cross-functional teams Fluent in English, written and spoken #J-18808-Ljbffr