Clinical Data Associate II

📋 Description

• Candidates can be based in Hungary, Poland, Romania, Serbia or Slovakia.
• Provide data management support for trials from start-up to post database lock.
• Follow SOPs, regulatory directives, and study plans.
• May develop CRF specs and coordinate stakeholder feedback.
• May build and test databases; perform UAT and maintain docs.
• Train staff on CRF, EDC, and project-related items as needed.

🎯 Requirements

• Bachelor's degree or related experience.
• Around 2 years experience as a Clinical Data Associate in CRO/Pharma/Biotech.
• MS Office proficiency: Word, Excel, PowerPoint, Outlook.
• Able to handle various clinical research tasks.
• Excellent organizational and communication skills.
• Professional English (written and oral).