Beschreibung
CRA for Scandinavian countries (m/f/d)
Reference: -en
Start: asap
Duration: 24 MM
Main tasks:
- Consulting and Communication of Regulatory tasks to do with the client´s study with the Swedish authorities/ethic authoritites
- Initiating the study itself
- CRA tasks such as monitoring of patients, comparing data in eCRF, visits and close out visits
Main qualifications
- CRA with experience in ISO 14155 or strong GCP Background
- Experience with medical devices and/or pharmaceutical products
- Area of expertise: at best with immunology or immunapheresis or neurology
- Experience with phases I-V
- Fluent in Swedish and English
Main advantages:
- You benefit from the exclusive access to interesting companies and exciting projects in collaboration with Hays as a solid and strong partner
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:
Alexander Chytraeus
Referencenumber:
Make contact:
Phone:
Email: