Empleos de ich en Madrid

Jobtailor in Barcelona, Spain, is seeking an experienced Medical Writer to compile and coordinate clinical documents, ensuring adherence to ICH E3 guidelines and regulatory standards. You will review study protocols, clinical study reports, manuscripts, and investigator brochures, manage editorial reviews, and collaborate with clients and internal teams to...

OverviewIn this CRA role, you monitor oncology/hematology trials and ensure adherence to ICH-GCP, local regulations, and SOPs. You collaborate with the Regional Clinical Operations Manager to meet study milestones and maintain data quality. You identify gaps, propose CAPAs, and support site start-up and local expertise. You work across sites to drive timely...

CROVELIS is seeking an experienced Clinical Research Associate to join our global clinical operations team, supporting international studies with high rigor and collaboration. You will monitor sites, ensure protocol compliance, and work with investigators and staff across multiple countries.The role demands strong GCP/ICH knowledge, independent site...

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...

Clinirx is expanding its clinical operations in Spain and seeks an experienced Clinical Research Associate to oversee site management and monitoring across trials. You will lead site initiation, monitoring visits, and close‑out activities, ensuring regulatory compliance and robust documentation. The role requires strong ICH-GCP knowledge, excellent...

How You'll Make An ImpactProvide technical consulting services that leverage Ecolab’s expertise in chromatography resin performance, downstream purification, and regulatory change management to help commercial teams understand customer needs and increase account revenue. Act as a pre-sales and customer-facing technical expert for Biopharma opportunities,...

Clinirx in Spain is seeking an experienced Clinical Research Associate (CRA) to support site management and monitoring across EU trials. You will handle initiation, routine monitoring, close-out visits, and regulatory/ethics documentation to ensure trial integrity.The ideal candidate has strong ICH-GCP knowledge, fluent Spanish and English, excellent...

AbbVie seeks a full-time, remote-position professional based in Madrid to execute clinical studies in line with ICH/GCP and regulatory standards. You will support the Study Project Manager, lead cross-functional study teams, and oversee CTMS and vendor relationships from Madrid.You will help develop study blueprints, create training for sites and vendors,...

Syneos Health in Madrid, Spain is seeking a Medical Writer to join future roles on clinical study or regulatory project teams. You will write, edit, and coordinate content for clinical/regulatory documents to ensure high-quality completion of all assigned writing projects.The role involves compiling documents such as study protocols, protocol amendments,...

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...

IQVIA is seeking a Global Study Associate Director to lead a cross-functional study team and oversee outsourced delivery for clinical studies in line with timelines, budget, and quality standards. The role requires ICH-GCP knowledge, strong leadership, and experience in study management across all phases. You will drive planning, risk management, and...

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...

Fortrea is seeking a Site Start-Up Specialist to coordinate site activation and regulatory submissions. You will manage essential documents, ensure ICH/GCP compliance, and submit country-specific forms with accuracy.The role involves collaboration with internal teams and external stakeholders, including regulatory authorities, to maintain audit-ready...

Agilent Technologies is seeking a Lead Internal Auditor within the Customer Quality & Compliance team. You will plan, lead, and execute risk-based internal audits across regulated medical devices and pharmaceutical environments, ensuring QMS compliance with ISO 9001/13485, FDA cGMP/QSR, EU GMP, IVDR, and ICH. You will also support inspection readiness, train...

Precision for Medicine is seeking a Clinical Research Associate II based in Madrid or Barcelona. You will monitor and own the progress of clinical studies at investigative sites, ensuring adherence to protocol, SOPs, ICH-GCP, and regulations. The role requires 4-year degree and 2+ years as CRA, site management experience, oncology monitoring, and a...

Compile, write, edit, and coordinate medical writing deliverables presenting scientific information clearly and accuratelyComplete clinical study protocols and protocol amendments, clinical study reports, patient narratives, and investigator brochuresApply regulatory standards, ICH E3 guidelines, SOPs, client standards, approved templates, authorship...

Syneos Health is seeking a Senior Medical Writer - Early Phase (Single Sponsor Support) in Madrid to lead the clear and accurate completion of medical writing deliverables for individual studies, coordinating activities across departments and responding to client comments.You will prepare protocols, clinical study reports, safety documents, and manuscripts,...

Indero is seeking a Clinical Trial Manager II to lead the operational management of investigative sites and oversee clinical trial deliverables. You will coordinate CRA activities, ensure adherence to SOPs and ICH/GCP guidelines, and develop action plans to address site performance concerns.You will mentor CRAs and junior staff, manage risk, budgets,...

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...

TFS HealthScience is seeking an Associate Director, Study Start Up, to manage country-level deliverables and timelines for clinical studies. This home-based role is essential in ensuring compliance and quality in study execution. The ideal candidate will have over 8 years of clinical research experience, including expertise in global clinical trials. The...