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CLINICAL RESEARCH ASSOCIATE (CRA)

Lombardia - Lombardia | PERM

Settore: Farmaceutica

Il nostro cliente
Clinical Research Organization

Descrizione
Reporting to the Head of CRO, the CRA will be responsible of:
·Oversee the progress of a Clinical Trial, ensuring that it is conducted, recorded and reported in accordance with the protocol, Standard Operating Procedures (SOPs), Good Clinical Practice (GCP) and the applicable Regulatory requirements;
·Interaction with internal teams;
·Willing to travel.

Profilo ricercato
Requirements:
·An enthusiastic and motivated individuals ready to learn;
·Able to work independently;
·Meet a variety of healthcare professionals at monitoring sites;
·Degree, or equivalent, in a scientific or healthcare discipline;
·At least 3 year of monitoring experience and strong expertise in a CRO or pharmaceutical environment.

Packages
Work from office or home, offering you total flexibility to manage your own time.
Fluent English is a must.

Contatto Michael Page
La vostra candidatura sarà trattata da Cristiano Pechy De Pechujfalu

Riferimento: OCPE181917