Clinical Trial Associate (m/f/d)

REFERENCE NUMBER:

419212/1

MY DUTIES:

-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

MY QUALIFICATIONS:

-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

MY BENEFITS:

-A very renowned company

ABOUT 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.

MY CONTACT AT HAYS:

My contact person
Selma Hrustic

Reference number
419212/1

Contact
E-Mail: [email protected]