CRA or Senior SCRA Russia (Clinical Research Associate)
Nr ref.: /JOBS.pl
The key responsibilities of a Clinical Research Associate (CRA/SCRA) are to perform the clinical monitoring aspect of designated projects in accordance with applicable SOP and regulations, performing clinical on-site monitoring activities, collecting regulatory documentation, performing qualification, initiation, monitoring and termination of investigational sites in accordance with ICH GCP guidelines.
Responsibilities & Accountabilities of a CRA/SCRA:
• Take responsibility for specific tasks on projects, or acts as the main CRA/SCRA contact on individual projects • Strong regulatory knowledge including GCP • Strong computer and internet skills including knowledge of MS-Office products such as Excel & Word. • Train team members on selected tasks
A successful CRA/SCRA candidate will:
• Have substantial monitoring experience within the field of clinical research • Be educated to a degree level in a life science • Be competent in both written and oral English • Have the ability to complete tasks in an accurate and timely manner.
If you are interested in this role, please send your CV to with your availability, or for a confidential conversation about the role please contact Simon on .
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