global start sl

A OnaCare busquem incorporar un/a Arquitecte/a a la nostra plantilla per supervisar i gestionar diferents obres dels nostres centres, donant suport a un nou projecte. Jornada: Completa. Funcions principalsSeguiment i supervisió de les obres als centres OnaCare. Coordinació amb empreses constructores, industrials i proveïdors. Control de terminis,...

A OnaCare busquem incorporar un/a Arquitecte/a a la nostra plantilla per supervisar i gestionar diferents obres dels nostres centres, donant suport a un nou projecte. Jornada: Completa. Funcions principalsSeguiment i supervisió de les obres als centres OnaCare. Coordinació amb empreses constructores, industrials i proveïdors. Control de terminis,...

A OnaCare busquem incorporar un/a Arquitecte/a a la nostra plantilla per supervisar i gestionar diferents obres dels nostres centres, donant suport a un nou projecte. Jornada: Completa. Funcions principals Seguiment i supervisió de les obres als centres OnaCare. Coordinació amb empreses constructores, industrials i proveïdors. Control de terminis,...

A OnaCare busquem incorporar un/a Arquitecte/a a la nostra plantilla per supervisar i gestionar diferents obres dels nostres centres, donant suport a un nou projecte. Jornada: Completa. Funcions principalsSeguiment i supervisió de les obres als centres OnaCare. Coordinació amb empreses constructores, industrials i proveïdors. Control de terminis,...

JBC Soldering Tools in Molins de Rei, Spain, seeks an experienced Electronics Purchasing Specialist to join the Purchasing Department.Siga leyendo para comprender completamente lo que este trabajo requiere en cuanto a habilidades y experiencia. Si su perfil encaja, presente su candidatura.You will source electronic components and manage supplier...

JBC Soldering Tools in Molins de Rei, Spain, seeks an experienced Electronics Purchasing Specialist to join the Purchasing Department.Siga leyendo para comprender completamente lo que este trabajo requiere en cuanto a habilidades y experiencia. Si su perfil encaja, presente su candidatura.You will source electronic components and manage supplier...

Hey there! Si los siguientes requisitos del puesto y la experiencia coinciden con sus habilidades, por favor, asegúrese de enviar su solicitud sin demora.We're Fever, the world's leading tech platform for culture and live entertainment. Our mission? To democratize access to culture and entertainment. With our proprietary cutting-edge technology and...

Parexel is seeking a Global Study Associate to join the FSP Clinical Operations team in Spain or Poland. This role supports Clinical Trial Managers across multiple study phases, ensuring GCP compliance and effective vendor oversight. You will handle TMF, site records, and cross-functional coordination to keep studies on track.You will work in a...

Parexel is seeking a Global Study Associate to join the FSP Clinical Operations team in Spain or Poland. This role supports Clinical Trial Managers across multiple study phases, ensuring GCP compliance and effective vendor oversight. You will handle TMF, site records, and cross-functional coordination to keep studies on track.You will work in a...

Parexel is seeking a Global Study Associate to join the FSP Clinical Operations team in Spain or Poland. This role supports Clinical Trial Managers across multiple study phases, ensuring GCP compliance and effective vendor oversight. You will handle TMF, site records, and cross-functional coordination to keep studies on track.You will work in a...

Parexel is seeking a Global Study Associate to join the FSP Clinical Operations team in Spain or Poland.Consulte la descripción del puesto a continuación. Si confía en que tiene las habilidades y la experiencia adecuadas, envíe su solicitud hoy mismo.This role supports Clinical Trial Managers across multiple study phases, ensuring GCP compliance and...

Parexel is seeking a Global Study Associate to join the FSP Clinical Operations team in Spain or Poland. This role supports Clinical Trial Managers across multiple study phases, ensuring GCP compliance and effective vendor oversight. You will handle TMF, site records, and cross-functional coordination to keep studies on track.You will work in a...

Parexel is seeking a Global Study Associate to join the FSP Clinical Operations team in Spain or Poland. This role supports Clinical Trial Managers across multiple study phases, ensuring GCP compliance and effective vendor oversight. You will handle TMF, site records, and cross-functional coordination to keep studies on track.You will work in a...

The Opportunity Puig is a major player in the worldwide fashion and beauty industry. We have a wide portfolio of well‑known luxury brands across fashion, fragrance, makeup, skincare, and wellness. Founded more than 100 years ago, Puig is a family‑owned company with a long‑term commitment to our brands and stakeholders. Puig is seeking a highly...

Vidoomy Media SL busca un Sales Account Manager para unirse a su equipo internacional de Client Success en Madrid. La posición implica servir a anunciantes y agencias de mercados diversos, planificar campañas clave y liderar su ejecución con apoyo de Adops.Se valorará experiencia en gestión de cuentas, planificación de medios y capacidad para analizar...

Lead regulatory strategy and submissions for clinical trials, coordinating applications and ensuring compliance for biotech and pharma companies. Requires extensive experience in regulatory submissions and CTIS.

Premier Research Group is seeking a Regulatory Submissions Lead II to join our Regulatory Submissions and Contracts team in Spain. You will lead and execute regulatory strategy, submissions, and approvals across multiple regions, coordinating CTAs, imports/exports, and complex regulatory packages for multi-region studies.You will act as the primary...

CTI Clinical Trial and Consulting Services is seeking an experienced Regulatory Affairs professional to support Study Start-Up (RASSU) activities across multiple countries. You will advise project teams on regulatory requirements and oversee submissions to IRBs/ECs, ensuring quality and compliance across sites.Responsibilities include adapting study...

CTI Clinical Trial and Consulting Services is seeking an experienced Regulatory Affairs professional to support Study Start-Up (RASSU) activities across multiple countries. You will advise project teams on regulatory requirements and oversee submissions to IRBs/ECs, ensuring quality and compliance across sites.Responsibilities include adapting study...

Hey there! Si los siguientes requisitos del puesto y la experiencia coinciden con sus habilidades, por favor, asegúrese de enviar su solicitud sin demora.We're Fever, the world's leading tech platform for culture and live entertainment.Our mission? To democratize access to culture and entertainment. With our proprietary cutting-edge technology and...