Clinical Trial Administrator II

📋 Description

• Prepare and assemble study docs for Regulatory Authorities and Ethics Committees.
• Manage electronic TMF setup and ongoing quality checks.
• Oversee CRO filing in the eTMF and ensure completeness.
• Support budget development, forecasting, and investigator fee reconciliation.
• Organize Kick Off Meetings and CRO study updates.
• Ensure trial activities comply with SOPs and quality standards.

🎯 Requirements

• Bachelor's degree.
• Experience in clinical research or healthcare incl. CTA.
• Knowledge of regulatory and ICH_GCP guidelines.
• Experience managing budgets, study documentation, and TMFs.
• Early-phase trial experience beneficial.
• Team collaboration and active contribution in a large group.