Empleos de icon en Barcelona

Overview In this role you drive delivery of innovative clinical research programs within ICON Biotech's General Medicine portfolio, with a dedicated focus on obesity studies. You lead cross-functional teams to deliver projects efficiently and compliantly, while developing team capability and stakeholder alignment. You will manage plans, timelines 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...

Experteer Overview Inscríbase (haciendo clic en el botón correspondiente) después de revisar toda la información relacionada con el trabajo a continuación. In this role you drive delivery of innovative clinical research programs within ICON Biotech's General Medicine portfolio, with a dedicated focus on obesity studies. You lead cross-functional teams...

Overview In this role you will support health economics and epidemiology research by analyzing observational study data and preparing deliverables. You will assist in study protocol development, analysis planning, data management, and synthesis of results for clients in pharma and medical devices. You work within a values-driven, collaborative team focused...

Overview In this role you oversee end-to-end site contracting for clinical trials, negotiating and tracking agreements and budgets. You will lead contract management workstreams, ensure quality and timely deliverables, and mentor Site Contracts Negotiators. You’ll collaborate with legal, finance, and project teams to align on contract language and risk....

Overview In this role you drive delivery of innovative clinical research programs within ICON Biotech's General Medicine portfolio, with a dedicated focus on obesity studies. You lead cross-functional teams to deliver projects efficiently and compliantly, while developing team capability and stakeholder alignment. You will manage plans, timelines and...

OverviewPuede obtener más detalles sobre la naturaleza de esta vacante y lo que se espera de los solicitantes leyendo la información a continuación.In this role you oversee end-to-end site contracting for clinical trials, negotiating and tracking agreements and budgets. You will lead contract management workstreams, ensure quality and timely deliverables,...

Overview As Site Specialist II at ICON, you support clinical trial sites in Spain to drive start-up, activation, and ongoing site management. You act as a key operational contact for Spanish investigator sites and internal study teams, ensuring regulatory activities, documentation, and milestones are managed accurately. The role requires hands-on EU CTR...

OverviewDé el siguiente paso en su carrera profesional ahora: desplácese hacia abajo para leer la descripción completa del puesto y envíe su solicitud.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...

Overview As Site Activation Lead, you drive study start-up from plan to activation, safeguarding timelines, budgets, and patient access. You’ll coordinate regulatory submissions, site contracts, and risk mitigation while guiding regional teams to align with sponsor expectations. This role sits at the heart of accelerating trial activation and patient...

Overview In this role you will coordinate and oversee clinical trial projects to ensure delivery on time, within budget and to high quality standards. You will lead cross-functional teams, manage plans, risks, and stakeholder expectations, and report progress to senior management. You will develop team capability and drive continuous improvement across...

Overview 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...

Overview As a Principal, Study Start Up Associate at ICON, you lead clinical trial start-up and site activation efforts to ensure regulatory compliance and timely activation. You will work with cross-functional teams to streamline processes and build start-up capability, guiding sites and study teams through early-phase activities. You’ll stay ahead of...

OverviewDescubra si esta oportunidad es adecuada para usted leyendo toda la información que sigue a continuación.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...

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 Principal Clinical Data Standards Consultant, you provide expert-level standards knowledge and shape ICON's standards content for internal and sponsor-facing projects. You will develop and maintain standards libraries compliant with CDISC and regulatory requirements, guiding data management activities. You collaborate across functions to define...

Principal Data Standards ConsultantICON 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...

Clinical Research Associate Home based BarcelonaICON 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,...

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...

POL-Start Up- HBICON 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.As a...