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...

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,...

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...

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...

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...

Almirall, S.A in Sant Feliu de Llobregat is seeking a QA Senior Manager to maintain and improve the GVP Quality Management System, ensuring compliance with ICH, EU GVP modules, and pharmacovigilance regulations.You will lead audits, inspections, and QA activities with internal and external partners, fostering continuous improvement while coordinating with...

Cytel Inc. is seeking a Senior/Principal Statistical Programmer (Remote) to work on sponsor projects embedded with a pharmaceutical client. You will lead SAS programming and collaborate with CROs to ensure data quality for submissions.You will implement SDTM/ADaM, develop datasets and tables, and support regulatory submissions while adhering to FDA/ICH and...

Cytel seeks a Senior/Principal Statistical Programmer for a sponsor-dedicated, fully remote role embedded with a global pharmaceutical client. You will oversee SDTM/ADaM work, define.Xml and reviewer’s guides, and deliver high-quality programming for regulatory submissions.You will develop SAS and R programs, supervise CRO deliverables, support study...

Cytel is seeking a Principal Statistical Programmer embedded with a leading pharmaceutical client. The role requires independent work, advanced SAS programming, and strong CDISC expertise to deliver datasets, tables, and listings for regulatory submissions.You will collaborate with CROs and internal teams, maintain standards, and contribute to study reports...

Cytel Inc. is seeking a Senior/Principal Statistical Programmer to work remotely on global pharmaceutical projects. You will develop SAS and R programs, generate SDTM/ADaM outputs, and oversee CRO programming to ensure timely, high-quality data delivery for regulatory submissions.You will work with FDA/ICH guidelines, contribute to study reports and...

Cytel Inc. is seeking a Senior/Principal Statistical Programmer SAS + R to join a sponsor-dedicated program, fully remote. You will generate SDTM/ADaM, develop SAS and R code, and oversee CROs to ensure high-quality data for multiple clinical trials.The role requires 7+ years in biotech/pharma, expert SAS, CDISC, and familiarity with FDA/ICH guidelines, with...

AbbVie seeks a qualified professional to execute and support clinical studies from Madrid in a remote capacity. The role requires SOP/ICH knowledge, regulatory compliance, and collaboration with cross-functional teams to ensure quality study conduct.Candidates should have 4+ years in pharma-related research and at least 3 years in trial management, with RN...

Cytel Inc. seeks a Senior/Principal Statistical Programmer for remote work, embedded with a pharmaceutical client. You will independently lead programming efforts, develop SDTM/ADaM specifications, and deliver high‑quality datasets, tables, and figures.Strong leadership and FDA/ICH knowledge are essential, with CRO oversight across multiple studies. The...

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...

Senior Medical WriterThe Senior Medical Writer independently plans and prepares a range of regulatory documents and medical communications to support all phases of product development. The primary responsibilities of the position are organizing, analyzing, interpreting, and presenting scientific and statistical information in accordance with International...

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...

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...

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...