For this project we are looking for a Clinical Research Associate (CRA).
The CRA performs monitoring activities related to initiation, conduct (recruitment, quality data collection) and timely completion of Phase I-IV Oncology and Pharma clinical trials within the country.
You are responsible to deliver data within timelines and required quality standard, responsible for adherence to monitoring procedures in accordance with GCP and ICH, local regulations and SOPs.
Sounds like a project for you? Please send your CV + motivation letter to : firstname.lastname@example.org