Responsible for study team agenda and meeting minutes and preparation
File and archive all study documents on Veeva Vault (eTMF) and ensure inspection readiness of the TMF
Verify vendor’s work order and create / update purchase orders accordingly
Ensure review of study budget
Contribute to the quality of all activities and key steps of the clinical study deliverables, according to GCP and SOP
Update and/or track study reporting tools
First previous experience as a Clinical Trial Associate
First experience in the Pharma industry
Being able to work fulltime on site in Lausanne
ETMF and Excel Knowledge
Eye for detail and eagerness to learn all the tools needed
Fluency in English
A very renowned company
Über Hays: With over 15 years of experience in the pharmaceutical industry, biotechnology and medical engineering, we know the key contacts at companies that are recruiting for challenging jobs with real potential. The current high demand for staff has opened up exciting opportunities for dedicated professionals looking to develop themselves professionally and to further their careers. As recruitment specialists with an international network of contacts, we can offer you decisive advantages – all completely free of charge. Register with us and reap the benefits of job offers that are both interesting and relevant to your skills and experience.
Diese Anzeige ist nur für angemeldete User möglich.
Bitte loggen Sie sich ein oder registrieren Sie sich, um sich auf das Projekt zu bewerben.