CRA II - Madrid

El operador/a cra es responsable de tramitar y gestionar señales de alarma derivadas de sistemas instalados en clientes. · Realizar video verificación remota y emisión de llamadas para gestión. · Controlar novedades e realizar tareas administrativas. · ...

We are currently seeking a Clinical Research Associate to join our diverse and dynamic team at ICON Plc.As a key member of our research department, you will be responsible for overseeing and coordinating clinical trials. · ...

+Job summary · We are currently seeking a Senior Clinical Research Associate (CRA) to join our diverse and dynamic team. +Advanced degree in a relevant field such as life sciences, nursing, or medicine. · +">Monitoring clinical trial sites to ensure adherence to study protocols r ...

We are currently seeking a Senior Clinical Research Associate (CRA) to join our diverse and dynamic team. · Monitoring clinical trial sites to ensure adherence to study protocols, regulatory requirements, and Good Clinical Practice (GCP) standards. · Conducting site visits to ass ...

We are currently seeking a Senior Clinical Research Associate (CRA) to join our diverse and dynamic team.We will play a critical role in overseeing and managing clinical trial activities to ensure they are conducted according to protocol, regulatory requirements, and industry sta ...

Se busca gestor CRA con experiencia en operativa y normativa A costumbrad@ a trabajar con MasterMind, Salesforce. · ...

Roles within Clinical Monitoring/CRA are responsible for overseeing and ensuring the integrity of clinical research studies by monitoring data and processes from a centralized location. · This includes conducting remote monitoring of trial sites to verify compliance with regulato ...

Clinical research associates oversee clinical trials by monitoring data and processes remotely, ensuring compliance with regulatory requirements. · ...

Buscas desarrollar tu talento en un lugar dónde tu esfuerzo sea reconocido. Te ofrecemos un entorno dinámico cercano y futuro. · ...

We are currently seeking a Clinical Research Associate II to join our diverse and dynamic team.As a Clinical Research Associate II at ICON, you will play a pivotal role in designing and analyzing clinical trials, interpreting complex medical data, and contributing to the advancem ...

We are currently seeking a Clinical Research Associate II to join our diverse and dynamic team. · ...

We are seeking a Clinical Research Associate II to join our diverse and dynamic team.We're proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development. · Conducting site quali ...

We have successfully supported the top 50 pharmaceutical companies and more than 750 biotechs. As part of our global team, you'll have the opportunity to perform and coordinate all aspects of the clinical monitoring process. · Monitors investigator sites with a risk-based monitor ...

This position involves overseeing clinical research studies by monitoring data and processes remotely. The CRA II will conduct site qualification visits ensuring compliance with regulatory requirements · Performs site qualification, site initiation, interim monitoring, · site man ...

We have successfully supported the top 50 pharmaceutical companies and more than 750 biotechs, spanning across countries in the last years. · ...

We have successfully supported the top 50 pharmaceutical companies and more than 750 biotechs, spanning 2, · 700 clinical trials across · 100+ countries in the last · 5 years. · Join Us as a Clinical Research Associate (Level II) – Make an Impact at the Forefront of Innovation · ...

We're proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development. · As a Clinical Research Associate II at ICON, you will play a pivotal role in designing and analyzing clini ...

Performs site qualification, site initiation, interim monitoring, site management activities and close-out visits (performed on-site or remotely) ensuring regulatory compliance. Verifies the process of obtaining informed consent has been adequately performed and documented for ea ...

We have successfully supported the top 50 pharmaceutical companies and more than 750 biotechs spanning clinical trials across countries in the last years. · ...

Se busca personal de seguridad para un servicio importante en Zamudio (Bizkaia), dentro del Parque Tecnológico. · ...