Empleos de icon en Barcelona

Clinical Project Manager - General Medicines, Obesity - ICON BiotechICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each...

As a Clinical Research Associate II at ICON, you contribute to designing and analyzing clinical trials and interpreting medical data to advance innovative therapies. You will oversee site qualification, initiation, monitoring, and close-out visits, ensuring protocol compliance, data integrity, and patient safety. You will collaborate with investigators and...

Siemens Digital Industries Software is a leading provider of solutions for the design, simulation, and manufacture of products across many different industries.Formula 1 cars, skyscrapers, ships, space exploration vehicles, and many of the objects we see in our daily lives are being conceived and manufactured using our Product Lifecycle Management (PLM)...

Clinical Project Manager - General Medicines, Obesity - ICON BiotechICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each...

Clinical Project Manager - General Medicines, Obesity - ICON BiotechICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each...

Overview You will empower real world evidence studies by designing analyses, programming in SAS and R, and delivering statistical outputs that support decision-making. In the BMW Real World Evidence team, you collaborate across biostatistics, medical writing, and stakeholders to shape study design, analysis plans, and scientific communications. You will...

Descripción del trabajoGlobal Study Manager ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers,...

JR158816 Senior Statistical AnalystICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers, patients and...

In this role you will design, implement, and validate SAS programs to support statistical analyses in clinical trials.¿Es este su próximo empleo? Descúbralo leyendo la descripción completa a continuación y no dude en enviar su candidatura.You will work closely with biostatisticians to shape analysis plans and ensure outputs meet scientific and...

Clinical Project Manager - General Medicines, Obesity - ICON BiotechICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each...

Overview As a CRA II at ICON, you monitor and support clinical trials to ensure quality, compliance, and patient safety. You will work with investigators and site staff to drive study conduct and data integrity, contributing to study documentation and reports. This home-based role in Barcelona offers meaningful exposure to cutting-edge therapies within a...

Experteer Overview In this role, you drive site engagement to support efficient clinical trials and ensure compliant study conduct. You will collaborate with trial sites and internal teams to tailor engagement strategies, monitor performance, and foster strong, compliant relationships. The position offers impact across multiple studies and sites,...

As Global Study Manager, you enable global hematology studies in collaboration with AstraZeneca, ensuring timely delivery, budget discipline, and high quality. You work within ICON’s FSP team to integrate with client operations and external vendors, driving study setup, execution, and close-out. You’ll contribute to risk management, QA, and inspection...

CRA IIICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers, patients and suppliers.We are currently...

Siemens Digital Industries Software is seeking a Digital Icon Artist / Illustrator to join our internal product design team. You will develop clear, polished experiences for our engineering software, creating 2D/3D icons and UI artwork that translate complex concepts into intuitive visuals.You will work with a globally distributed UX team across multiple...

CRA IIICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers, patients and suppliers.We are currently...

ICON Clinical Plc busca un profesional para impulsar la participación de sitios y apoyar ensayos clínicos eficientes, asegurando el cumplimiento de las normativas y la calidad de los datos. Trabajarás en estrecha colaboración con sitios y equipos internos para adaptar estrategias de compromiso, monitorizar el rendimiento y garantizar relaciones sólidas...

Overview In this role you will oversee and drive the conduct of clinical trials to ensure alignment with protocol, GCP, and regulatory standards. You will monitor sites, manage data integrity, and support cross-functional teams to enable compliant, timely trial execution. You’ll train site staff, build strong relationships with stakeholders, and travel as...

Overview As Global Study Manager, you enable global hematology studies in collaboration with AstraZeneca, ensuring timely delivery, budget discipline, and high quality. You work within ICON’s FSP team to integrate with client operations and external vendors, driving study setup, execution, and close-out. You’ll contribute to risk management, QA, and...

Overview In this role you drive high-quality regulatory and clinical documents, leading writing workstreams and cross-functional collaboration to support major submissions. You guide best practices, mentor junior writers, and stay aligned with evolving regulatory standards. You act as the lead writer on complex projects, shaping regulatory submissions for...