🛠 Tech Stack

💼 About This Role

You'll review source data and ensure its completeness and accuracy for clinical trials at Celerion, a translational medicine company. You'll perform quality control of case report forms and data entry into databases, ensuring compliance with GCP and FDA guidelines.

🎯 What You'll Do

• Review source documents and case report forms for accuracy
• Perform ongoing quality control of clinical source data
• Enter and verify data in sponsor-provided EDCs
• Archive source documentation and complete QC milestones

📋 Requirements

• High school diploma or GED
• 1-2 years industry experience preferred
• Proficiency in MS Office applications
• Excellent attention to detail

✨ Nice to Have

• Medical terminology training
• Quality control or data entry experience
• Relevant internal Celerion experience

🚩 Heads Up

• Lists both 'preferred' and 'required' experience inconsistently
• High school diploma as minimum education for clinical data role