As a Clinical Trial Assistant you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.

This CTA role is dedicated to one client and is partially office based. This role is based in Bratislava and assumes 3 days in the office.

CTA assists in the coordination and administration of the study activities from the start up to execution and close out, and within the Local Study Team to ensure quality and consistency of interventional study deliverables to time, cost and quality objectives.

• Coordination and administration of clinical studies from the start-up to execution and close-out
• Collects, assists in preparation, reviews and tracks documents for the application process. Assists in timely submission of proper application/documents 
• Interfaces with Investigators, external service providers and CRAs during the document collection process to support effective delivery of a study and its documents.
• Serves as local administrative main contact and works closely with the CRAs and other members of the team for the duration of the study.
• Operational responsibility for the correct set-up and maintenance of the local eTMF and ISF including document tracking in accordance with ICH-GCP and local requirements.
• Ensures essential documents under their responsibility are uploaded in a timely manner to maintain the eTMF “Inspection Readiness”.
• Ensures that all study documents are ready for final archiving and completion of local part of the eTMF and supports the CRA in the close out activities for the ISF

#LI-NR1

• Bachelor of Science or equivalent - FRESH GRADUATES ARE WELCOME
• Time management skills 
• Teamplayer 

• MS office  proficient