Beschreibung:For one of our Pharma clients we are seeking freelance support as:CRA Clinical Research Associate (M/F) home based in Portugal or Finland
Assisting in initiating trial implementation including preparation of Ethics Committee/Institutional Review Board materials and communicating approval
Ensure clinical trials are conducted in a timely manner and in accordance with Standard Operating Procedures, the principles of ICH/Good Clinical Practice and all applicable regulations governing the conduct of clinical trials.
Managing, implementing and monitoring clinical studies in a team setting.
Verify that the rights and well-being of human subjects are protected and that the reported trial data are accurate, complete, and verifiable from source documents
Monitor responsibilities include: manage assigned clinical study protocols and amendments; track deviations; manage clinical trial sites and assure timely initiation and completion of clinical studies.
Medical or science education
1-2 years experience in clinical monitoring within the medical device or pharmaceutical industry
Knowledge of medical practice/techniques and terminology.
Knowledge of European regulations governing clinical trials.