Empleos de ich en Madrid

Si estás preparado para liderar la reinvención total de la empresa a través de la tecnología y los datos, tienes una oportunidad para unirte al equipo de Accenture y cambiar el futuro de nuestros clientes y la sociedad.Buscamos HR Transformation Consultant para unirse a nuestro Intelligent Consulting Hub en Barcelona y Madrid.Si tienes pasión por el...

Kymos-Group in Spain is seeking a Stability Scientist to join our Chemical Analysis and Quality Control Department in Cataluña. You will oversee ICH-compliant stability studies and related programs, coordinating with clients to ensure timelines and data integrity. Responsibilities include preparing protocols and reports, writing certificates of analysis,...

Si estás preparado para liderar la reinvención total de la empresa a través de la tecnología y los datos, tienes una oportunidad para unirte al equipo de Accenture y cambiar el futuro de nuestros clientes y la sociedad.Buscamos HR Transformation Consultant para unirse a nuestro Intelligent Consulting Hub en Barcelona y Madrid.Si tienes pasión por el...

Syneos Health in Madrid (or Barcelona) seeks a CRA II (Multisponsor) to perform site qualification, initiation, monitoring, and close-out visits, ensuring ICH-GCP compliance. Work can be on-site or remote per project, with hybrid schedules in Spain. Bachelor’s degree or RN plus 1 year independent on-site monitoring experience; strong knowledge of GCP/ICH...

Airline industry company located in the centre of MadridSettlement Standardization AnalystThe hiring company is a well-established organization within the Transport & Distribution industry. With a structured and professional approach, they provide a solid platform for growth and development in their accounting and finance department.Ensure the execution of...

IQVIA in Barcelona is seeking a Senior Clinical Research Associate to join our sponsor-dedicated CRA team. You will support multicenter trials, perform site visits, and help ensure GCP/ICH compliance throughout study conduct.Responsibilities include site initiation, monitoring, close-out visits, and managing recruitment plans. Strong English/Spanish, MS...

Medical Staff Talent is seeking a Senior/Principal Statistical Programmer to work remotely on pharmaceutical clinical development programs. You will implement reporting and analysis activities, lead SAS and/or R programming efforts, and oversee CRO programmers to ensure high-quality data outputs.You will collaborate with multiple study teams, contribute to...

Medicine moves forward here. Ergomedis a specialist clinical research organization focused on rarediseaseand select oncology indications. The Specialist, Study Start Up and Regulatory Affairs leads and coordinates all activities relatedcompliance, and serves as a key liaison between internal teams, clients, and external stakeholdersLeads study start-up and...

START Center for Cancer Research, con sede en Madrid, busca un/a Investigador/a Clínico/a para liderar y supervisar ensayos clínicos oncológicos, asegurando el cumplimiento de ICH-GCP y normativa aplicable. La persona gestionará estudios, velando por la seguridad de los pacientes y la calidad de los datos, en estrecha colaboración con sponsors y...

Crovelis busca un/a Gerente de Proyecto Clínico Senior para dirigir ensayos clínicos en Madrid. El candidato ideal tiene un grado en Ciencias de la Vida y más de 5 años de experiencia en investigación clínica. Esta posición implica la gestión de equipos multifuncionales y la responsabilidad de la ejecución conforme a las regulaciones ICH-GCP. Se...

Inbrain Neuroelectronics seeks a Clinical Research Coordinator to support planning, start-up, tracking, and operational activities for clinical investigations.You will collaborate with CROs, vendors, and investigational sites while maintaining TMF documentation and ensuring compliance with ICH-GCP and MDR requirements.The role emphasizes data quality, study...

TheClinical Research Associateis responsible for managing and monitoring clinical trials to ensure they are conducted in compliance with study protocols, ICH-GCP, and applicable regulations. This includes site selection, initiation, monitoring, and close-out activities, while ensuring data quality and patient safety. The role reports to the Clinical Project...

Syneos Health in Madrid is seeking a CRA II for sponsor-dedicated studies with experience in gastroenterology and genitourinary trials.The role emphasizes site qualification, monitoring, and close collaboration with study teams to ensure regulatory compliance and data integrity in real-world late phase environments. Strong knowledge of ICH-GCP and informed...

Chemo is seeking a Regulatory Affairs Associate for International Markets to join our Madrid team. You will coordinate regulatory dossiers across multiple territories, manage submissions, and support lifecycle activities, ensuring regulatory compliance throughout the product lifecycle in a dynamic, international environment.We expect 3–4 years of...

IBIMA Plataforma BIONAND in Málaga, Spain, seeks a Researcher with 4+ years in Neurology clinical trials and hands-on sample handling expertise.The role requires ICH GCP E6 (R3) training and knowledge of shipping hazardous materials.A nursing degree is required, with a 35-hour week under a Scientific-technical activities contract.The project funds 6 months,...

Cytel Inc. is seeking a Senior/Principal Statistical Programmer (SAS + R) for a fully remote role supporting a pharmaceutical client. You will lead SDTM/ADaM data handling, develop complex tables and graphs, and guide CRO programmers to ensure high-quality, compliant outputs for regulatory submissions.The role requires 7+ years in biotech/pharma programming,...

Cytel is seeking a Senior/Principal Statistical Programmer (Remote) to join our sponsor-dedicated, embedded team supporting global pharmaceutical clients. You will independently manage programming deliverables, develop SAS/R pipelines, and oversee CROs to ensure high-quality data outputs for submissions.You will work on SDTM/ADaM specifications, create...

Cytel Inc. is seeking a Senior/Principal Statistical Programmer for a fully remote role embedded with a global pharmaceutical client. You will lead statistical programming across SDTM/ADaM, Generate define.Xml and review guides, and oversee CRO deliverables in a fast-paced environment.You will apply extensive SAS and R expertise, ensure FDA/ICH compliance,...

Cytel Inc. is seeking a Senior/Principal Statistical Programmer (Remote) to lead programming activities across clinical development programs. You will generate SDTM/ADaM specifications, develop SAS code, and deliver complex analyses while collaborating with CROs and internal teams.The role requires extensive CDISC expertise, independent work, and strong...

Almirall, S.A. cerca uno/una QA Specialist per supportare il mantenimento e l’aggiornamento del Quality Management System per farmacovigilanza, in conformità a EU GVP, ICH e normative di settore.Lavorerai a stretto contatto con il QA GVP Senior Manager per assicurare ispezioni e audit efficaci a livello corporate e affiliate. È richiesto titolo in Life...