OBS! Ansökningsperioden för denna annonsen har
passerat.
Arbetsbeskrivning
Location: Slough, Berkshire
Details: Must be a graduate, postgraduate, 4 year college degree, or equivalent ideally in a scientific of healthcare discipline.Must have a minimum of 5 years experience of clinical trial regulatory affairs either in CRO or pharmaceutical industry.Must demonstrate an excellent knowledge ICH-GCP.Will act as the RAPM for designated complex projects and manage the regulatory affairs aspect of the project.Will participate in all departmental project related activities, will produce global clinical trial applications, clinical study reports, publications and summary documents.Full job description available.
Please send your application as soon as possible.
Vill du ha en längre platsbeskrivning?OBS!Ange i mailet att du önskar få platsbeskrivningen.
Information om att leva och bo i Storbritannien kan du hitta på www.ams.se och på www.eures.europa.eu
Denna tjänst kommer via EURES-nätverket (EURopean Employment Services).EU/EES-medborgare behöver inget arbetstillstånd.