Clinical Research Associate
Job in pharma for an important pharmaceutical company is looking for a CRA.
The position is office based:
Mendrisio, Switzerland
Job description
Acting as Clinical Research Associate (CRA) and assisting Clinical Project Leaders (CPL)Perform site qualification, initiation, interim monitoring, and/or close out monitoring visits in European clinical sites (mainly for sites located in Italy and Switzerland)Support in the management of National and International Phase I - Phase III clinical studiesSupport in the preparation of submission packages and documents submission to Regulatory AuthoritiesDirect contact with study Sponsors, Investigators, CPLs and Quality assurance to ensure that all documents are scientifically sound, well-organised, accurate, consistent, and in compliance with the applicable company SOPs and regulationsFiling and archiving of clinical study documentationand files
Other responsibilities
Assist in the preparation of study documentsSupport the CPL in training and management of study sites on all clinical aspects of the studySupport the CPL in the review of study monitoring documents
Job requirements:
A BSc or higher degree in a biomedical or other life science disciplineAt least 2 full years of experience in the roleCRA certification in accordance with the Italian DM 15. 11. 2012Competent in written and oral EnglishFluency in another language would be a plusAbility to work independently, directly interacting with other people internally and externally, and to meet deadlinesAbility to manage multiple priorities simultaneouslyProficiency in Microsoft Office Informazioni aggiuntive:
Lavoro da remoto:
Completamente di personaTipo di impiego:
Tempo pieno
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