Trabajo de Pharmacovigilance en Valencia

¡Be part of the future of drug safety at Asphalion! We're looking for a Pharmacovigilance Specialist ready to embrace new challenges in a fast-moving, international environment. If you thrive on precision and want to make a real impact, we'd love to have you on our team! Aumente sus posibilidades de llegar a la fase de entrevista leyendo la descripción completa del puesto y enviando su solicitud...

Due to our ongoing global expansion, we have a great opportunity for a Regulatory Submissions Specialist to join our growing regulatory team in Taiwan, on a fully remote basis. Inscríbase ahora, lea los detalles del trabajo desplazándose hacia abajo. Verifique que posee las habilidades necesarias antes de enviar una solicitud. We are looking for someone who can autonomously carry on the work...

In a nutshellPosition: Clinical Study CoordinatorLocation: Madrid, HibridExperience: 4+ years in international clinical trial coordinationWant to know more? mAbxience is a global biopharmaceutical company committed to innovation and excellence in the development and manufacturing of biotechnological medicines. We operate with a strong focus on quality, regulatory compliance, and scientific rigor...

Quality Control (QC) Technician – Biologics - Morning Shift 6am-2pmWe are seeking a highly motivated and detail-oriented Quality Control Technician to join our team, specializing in the analysis of biological products. This role involves hands-on laboratory work, project management, and technical oversight in a GMP-regulated environment.Key Responsibilities:Design, supervise, and execute quality...

We are currently looking for an experienced Safety Physician to support ongoing and upcoming clinical development projects. This role requires a highly competent professional with strong expertise across Clinical Safety and Pharmacovigilance, contributing both operationally and strategically. Key responsibilities will include:Providing comprehensive safety oversight across early- and late-stage...

To strengthen our Commercial Affiliate in Spain, we are currently hiring Si le interesa solicitar este empleo, por favor, asegúrese de cumplir los siguientes requisitos que se enumeran a continuación. Key Account Manager (m / f / x) – Immunology / Rare Diseases To cover either the North or the South of Spain - ideally located in Galicia / Zona Norte OR Alicante / Valencia Fulltime / permanent /...

We are currently looking for an experienced Safety Physician to support ongoing and upcoming clinical development projects. This role requires a highly competent professional with strong expertise across Clinical Safety and Pharmacovigilance, contributing both operationally and strategically.Key responsibilities will include:Providing comprehensive safety oversight across early- and late-stage...

The Senior Clinical Project Manager reports to the Clinical Operations Manager and is responsible to manage the local and international projects in compliance with contractual requirements, timelines, standard operating procedures and relevant regulations and legislations. He/she leads the internal study team allocated on his/her projects ensuring that all deliverables meet agreed expectations...

¡Be part of the future of drug safety at Asphalion! We're looking for a Pharmacovigilance Specialist ready to embrace new challenges in a fast-moving, international environment. If you thrive on precision and want to make a real impact, we'd love to have you on our team! Main responsibilities:Perform weekly global/local literature assessments.Efficiently manage Individual Case Safety Reports...

In a nutshell Sea uno de los primeros solicitantes, lea la descripción completa del puesto a continuación y luego envíe su candidatura para que sea considerada. Position: Clinical Study Coordinator Location: Madrid, Hybrid Experience: 4+ years in international clinical trial coordination Want to know more? mAbxience is a global biopharmaceutical company committed to innovation and excellence in...

The Senior Clinical Project Manager reports to the Clinical Operations Manager and is responsible to manage the local and international projects in compliance with contractual requirements, timelines, standard operating procedures and relevant regulations and legislations. He/she leads the internal study team allocated on his/her projects ensuring that all deliverables meet agreed expectations...

Due to our ongoing global expansion, we have a great opportunity for a Regulatory Submissions Specialist to join our growing regulatory team in Taiwan, on a fully remote basis.The Regulatory Submissions Specialist contributes to the management and development of procedures related to the activities in which he/she is involved in and ensures that the outputs of their activities meet the quality...

Overview Due to our ongoing global expansion, we have a great opportunity for a Regulatory Submissions Specialist to join our growing regulatory team in Taiwan, on a fully remote basis. Las cualificaciones, habilidades y toda la experiencia relevante necesaria para este puesto se pueden encontrar en la descripción completa a continuación. The Regulatory Submissions Specialist contributes to the...