Empleos de study start up associate director en Barcelona

Location: Barcelona - Spain (3 days working from the office and 2 days working from home) Introduction to the role The Study Start-Up Associate Director (SSU AD) is responsible for organizing, overseeing, and controlling the regulatory and ethics committee (EC) start-up processes for clinical trials conducted by Site Management & Monitoring (SMM) at the...

Experteer Overview Envíe su CV y cualquier información adicional requerida después de haber leído esta descripción, haciendo clic en el botón de solicitud. As Study Start-Up Associate Director, you will lead regulatory and Ethics Committee start-up activities for local trials within Site Management u0026amp; Monitoring. You will manage the SSU team,...

Location: Compruebe que cumple con los requisitos de habilidades para este puesto, así como con la experiencia asociada, y luego envíe su CV a continuación. Barcelona - Spain (3 days working from the office and 2 days working from home) Introduction to the role The Study Start-Up Associate Director (SSU AD) is responsible for organizing, overseeing, and...

Posted date Oct. 07, 2026 Contract type Full time Job ID R-261361 ## **Why choose AstraZeneca Spain?** AstraZeneca Spain is a rising force in our global business. With headquarters in Madrid and our global hub in Barcelona, we’ve become an important international centre of excellence in the fight against critical disease. Boasting vibrant...

**Location:** Barcelona - Spain (3 days working from the office and 2 days working from home) **Introduction to the role** The Study Start-Up Associate Director (SSU AD) is responsible for organizing, overseeing, and controlling the regulatory and ethics committee (EC) start-up processes for clinical trials conducted by Site Management & Monitoring...

AstraZeneca plc in Barcelona, Spain is seeking an Study Start-Up Associate Director to lead regulatory and Ethics Committee start-up activities for country-level trials within SMM. You will oversee the SSU team, ensure alignment with ICH-GCP, AZ procedures, and local regulations, and drive continuous process improvement. The role requires strategic...

AstraZeneca plc in Barcelona, Spain is seeking an Study Start-Up Associate Director to lead regulatory and Ethics Committee start-up activities for country-level trials within SMM. Desplácese hacia abajo para encontrar una descripción detallada de este trabajo y lo que se espera de los candidatos. Envíe su solicitud haciendo clic en el botón "Solicitar"....

Ergomed Group is a specialist clinical research organization focused on rare disease and select oncology indications, with global presence and a collaborative culture. The Specialist, Study Start Up and Regulatory Affairs leads and coordinates all activities related to achieving site initiation readiness and regulatory compliance. Role requires a graduate...

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...

The Global Study Associate Director (GSAD) is a business-critical role within Study Management, BioPharmaceuticals Clinical Operations, whose main accountability is the delivery of clinical studies. The GSAD is responsible for leading a cross-functional study team and for providing the team with direction and guidance to enable successful study delivery. The...

Job Overview Associate Clinical Project Management Directors supervise, manage and provide oversight to assigned Clinical Project Management staff who manage or support studies and/or programs to ensure delivery; time and quality resulting in strong financial performance and customer satisfaction. Manage direct reports and teams in accordance with...

Job Overview Associate Clinical Project Management Directors supervise, manage and provide oversight to assigned Clinical Project Management staff who manage or support studies and/or programs to ensure delivery; time and quality resulting in strong financial performance and customer satisfaction. Manage direct reports and teams in accordance with...

The Global Study Associate Director (GSAD) is a business-critical role within Study Management, BioPharmaceuticals Clinical Operations, whose main accountability is the delivery of clinical studies. The GSAD is responsible for leading a cross-functional study team and for providing the team with direction and guidance to enable successful study delivery. The...

ICON Strategic Solutions is seeking a Study Start Up Associate based in Spain with a home-based setup. You will lead initiation of clinical trials and ensure regulatory compliance to advance innovative therapies. The role requires a life sciences degree and at least 2 years of clinical research or regulatory affairs experience, with strong organizational and...

Advanced Clinical is seeking an experienced Study Site Specialist to manage site start-up activities in Spain.This fully remote permanent role requires coordinating documentation, regulatory submissions, and site activation from identification through regulatory clearance.You will lead feasibility, contract discussions, and oversight of regulatory...

## Global Study Associate ManagerBarcelona,, SpainApply NowFind out how well you match with this jobThe Global Study Associate Manager (GSAM) is a role within Development Operations and is a member of the global study team supporting the delivery of clinical studies from Clinical Study Protocol (CSP) development through study set-up, maintenance, close-out,...

The Global Study Associate Manager (GSAM) is a role within Development Operations and is a member of the global study team supporting the delivery of clinical studies from Clinical Study Protocol (CSP) development through study set-up, maintenance, close-out, development of the Clinical Study Report (CSR), and study archiving. The GSAM works with internal...

The Global Study Associate (GSA) is a member of the extended Global Study Team, supporting the delivery of clinical studies within Late Development Oncology (LDO) to time, cost, and quality standards. The GSA supports clinical studies throughout their lifecycle, from Clinical Study Protocol (CSP) development and study set-up through maintenance, close-out,...

IQVIA seeks a Global Study Associate Director (GSAD) to lead cross-functional study teams across clinical operations, ensuring delivery of studies on time, within budget and to high quality standards.Los candidatos deben tomarse el tiempo de leer atentamente todos los elementos de este anuncio de empleo. Por favor, envíen su solicitud sin demora.The GSAD...

Role Barcelona onsite 3 days office/2 days homeWould you like to be part of a fast-paced and agile global team that has direct strategic impact on drug development, empowered and trusted to innovate and experiment? Join us at AstraZeneca CVRM (Cardiovascular Renal Metabolism) Biometrics to impact a wide range of engaging projects striving to make a...