Empleos de start up en Barcelona

At Allucent™, we are dedicated to helping small-medium biopharmaceutical companies efficiently navigate the complex world of clinical trials to bring life-changing therapies to patients in need across the globe. We are looking for a Start-Up Associate Contractor to join our A-team (hybrid*/remote) for 0.5 Fte! The SUA coordinates and performs local site...

Uplift People Consulting seeks an Automation Engineer to analyze, design, and program automated systems for industrial machinery in a European market. You will lead start-up and commissioning, develop PLC/SCADA programs, and integrate external equipment to deliver reliable automation solutions.The role requires a Bachelor in Automation, Electrical, or...

IQVIA is seeking a senior professional to lead global study start-up, site activation, and regulatory activities.La descripción completa del puesto cubre todas las habilidades asociadas, la experiencia previa y cualquier cualificación que se espera que tengan los solicitantes.You will coordinate cross-functional teams, align timelines and budgets, and...

In this role you lead global study start-up, site activation, and regulatory activities to ensure compliant, timely delivery of clinical trials. You will align cross-functional teams, manage timelines and budgets, and oversee regulatory submissions across regions. You’ll mentor teams, support business development, and optimize processes within CTMS and...

Engineering Oil & Gas Company is seeking a Commissioning Electrical Supervisor for offshore projects with assignments in the Indonesia and Romania regions.Si los siguientes requisitos del puesto y la experiencia coinciden con sus habilidades, por favor, asegúrese de enviar su solicitud sin demora.The role focuses on safe commissioning, start-up and...

IQVIA is seeking a Site Contract Manager to develop local contracting strategy and support start-up contracting activities for selected sponsors, studies or multi-protocol programs.The role requires 3-5 years of sponsor or CRO site contracting experience, strong negotiation and writing skills, and a solid understanding of the regulated clinical trial...

Roche seeks a Clinical Site Manager specialised in Study Start-Up to lead end-to-end initiation activities at assigned sites, ensuring regulatory compliance and on-time delivery. You will manage EC/CA submissions, develop essential study documents, and collaborate with global and local teams to drive high-quality diagnostics trials while supporting an...

Job OverviewPerform tasks at a country level associated with Site Activation (SA) activities in accordance with applicable local and/or international regulations, standard operating procedures (SOPs), project requirements and contractual/budgetary guidelines. May also include maintenance activities.Essential FunctionsUnder general supervision, serve as...

Roche is seeking an experienced professional to lead end-to-end study start-up activities, including site activation and qualification assessments. You will manage EC/CA submissions and oversee CRO performance while serving as the clinical trial expert for site personnel.You’ll collaborate with global and local teams to ensure regulatory compliance,...

The Site Activation Partner is responsible for leading or supporting operational activities from start-up to close-out, for assigned studies and investigator sites to ensure compliance with study timelines and in accordance with prevailing laws, Good Clinical Practices, and sponsor standards. Other duties to include but not limited to: Initiate and...

Job Overview Perform tasks at a country level associated with Site Activation (SA) activities in accordance with applicable local and/or international regulations, standard operating procedures (SOPs), project requirements and contractual/budgetary guidelines. May also include maintenance activities. Essential Functions Under general supervision,...

IQVIA is seeking a senior professional to lead global study start-up, site activation, and regulatory activities. You will coordinate cross-functional teams, align timelines and budgets, and oversee regulatory submissions across regions to ensure timely delivery of clinical trials.You will mentor teams, support business development, and optimize processes...

Uplift People Consulting seeks an Automation Engineer to analyze, design, and program automated systems for industrial machinery in a European market. You will lead start-up and commissioning, develop PLC/SCADA programs, and integrate external equipment to deliver reliable automation solutions.The role requires a Bachelor in Automation, Electrical, or...

Roche is seeking an experienced professional to lead end-to-end study start-up activities, including site activation and qualification assessments. You will manage EC/CA submissions and oversee CRO performance while serving as the clinical trial expert for site personnel.You’ll collaborate with global and local teams to ensure regulatory compliance,...

At Roche you can show up as yourself, embraced for the unique qualities you bring. This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come. As a Clinical Site Manager specialising in Study Start-Up, you will be responsible for designing, planning, coordinating, and conducting all...

IQVIA is seeking a senior professional to lead global study start-up, site activation, and regulatory activities. You will coordinate cross-functional teams, align timelines and budgets, and oversee regulatory submissions across regions to ensure timely delivery of clinical trials.You will mentor teams, support business development, and optimize processes...

In this role you lead global study start-up, site activation, and regulatory activities to ensure compliant, timely delivery of clinical trials. You will align cross-functional teams, manage timelines and budgets, and oversee regulatory submissions across regions. You’ll mentor teams, support business development, and optimize processes within CTMS and...

Roche is seeking an experienced professional to lead end-to-end study start-up activities, including site activation and qualification assessments. You will manage EC/CA submissions and oversee CRO performance while serving as the clinical trial expert for site personnel.You’ll collaborate with global and local teams to ensure regulatory compliance,...

Job OverviewPerform tasks at a country level associated with Site Activation (SA) activities in accordance with applicable local and/or international regulations, standard operating procedures (SOPs), project requirements and contractual/budgetary guidelines. May also include maintenance activities.Essential FunctionsUnder general supervision, serve as...

Barcelona, Spain | Full time | Home-based | R1564053¿Está considerando presentar su candidatura para este trabajo? Compruebe todos los detalles en esta descripción del puesto y luego haga clic en "Solicitar".Key Responsibilities- Lead global and regional site activation and regulatory activities from study start-up through maintenance phases.- Develop and...