CRA Sponsor Based Temp

Responsibilities:

-Conducting trial/site management in accordance with protocol, SOPs, ICH-GCP guidelines and local legislation: obtaining necessary approvals and documentation, site initiations, monitoring and SDV, management of site recruitment performance, trial supplies management, handling of safety information, data cleaning activities, close-out and archiving
-Achieving close liaison with Project Management, Data Management and HQ throughout the trial to ensure milestones achieved
-Maintaining current knowledge of SOP’s, ICH GCP guidelines, local legislation and therapeutic areas

Descripción del Puesto 

Oportunidad para trabajar sponsor-dedicated & office-based en Madrid. Ensayos Clínicos fase II & III internacionales.

 

 

Responsabilidades 

Responsibilities:

-Conducting trial/site management in accordance with protocol, SOPs, ICH-GCP guidelines and local legislation: obtaining necessary approvals and documentation, site initiations, monitoring and SDV, management of site recruitment performance, trial supplies management, handling of safety information, data cleaning activities, close-out and archiving
-Achieving close liaison with Project Management, Data Management and HQ throughout the trial to ensure milestones achieved
-Maintaining current knowledge of SOP’s, ICH GCP guidelines, local legislation and therapeutic areas

Perfil 

Licenciatura en Ciencias de la Salud.
Formación complementaria en Monitorización de Ensayos Clínicos.
Inglés -advanced level mínimo-
Experiencia previa como CRA mínimo 1 año, DESEABLE 1.5-2.5 años.
(Se podrán valorarán perfiles trainee con experiencia concreta en SIV, MV y SCVs, a quienes en sus prácticas se las hayan delegado responsabilidades)

Información del Contacto 

Application form : CRA Sponsor Based Temp

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Files must be less than 3 MB.
Allowed file types: txt rtf html pdf doc docx odt.
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