Clinical Study Administrator Pharma

hace 1 semana


Madrid, España Page Personnel España A tiempo completo

Assists in coordination and administration of clinical studies from the start-up to execution and close-out. - Interfaces with Investigators, external service providers and CRAs during the document collection process to support effective delivery of a study and its documents. - Serves as local administrative main contact and works closely with the CRAs and/or the LSM for the duration of the study. - Ensures essential documents under their responsibility are uploaded in a timely manner to maintain the eTMF "Inspection Readiness". - Ensures that all study documents are ready for final archiving and completion of local part of the eTMF and supports the CRA in the close out activities for the ISF. - Contributes to the production and maintenance of study documents, ensuring template and version compliance. Multinational Pharmaceutical company|Clinical Study Administrator - University degree. - More than two years of experience as a Clinical Study Administrator or CTA within Pharmaceutical Industry. - Previous administrative experience preferably in the medical/ life science field. - High English level. - Open to work in a temporary contract. Multinational Pharmaceutical company. Good opportunity to join one of the best pharmaceutical company in the world. Multinational Pharmaceutical company is looking for a Clinical Study Administrator, in a temporary contract, based in Madrid. Clinical Study Administrator Pharma - Temporary contract



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