Description
Clinical Trial Assistant (m/f)
Reference: -en
Start: asap
Duration: 12 MM++
Main tasks:
- Support the Trial Management team in all phases of the clinical study conduct
- Assist in the coordination of meetings of the clinical project management team
- Set up and maintain protocols and site level trackers
- Preparation of site related documents and Investigator Site Files
- Track and distribute trial supplies
- Update clinical trial and clinical study systems and upload documents into systems
- Perform quality checks and reviews of the Trial Master File (TMF) and study reports
Main qualifications
- Experience in clinical development
- Previous experience in administration of clinical trials
- Knowledge of ICH and GCP
- Fluency in English
- Working knowledge of electronic Trial Master File, clinical trial portals and clinical trial management systems
Main advantages:
- A very renowned company
About us:
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:
Cigdem Aydin
Referencenumber:
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