🛠 Tech Stack

💼 About This Role

You'll lead enterprise-level data standardization and validation frameworks for clinical trials, ensuring regulatory compliance and data integrity. You'll architect scalable solutions in Python, R, SQL, and SAS, and mentor junior engineers. This role offers the opportunity to shape global clinical data systems at a growing CRO.

🎯 What You'll Do

• Develop enterprise data mapping strategies for analytics.
• Design validation frameworks to detect systemic data issues.
• Build modular codebases using Python, R, SQL, and SAS.
• Lead compliance initiatives for GCP and FDA 21 CFR Part 11.

📋 Requirements

• Bachelor's degree in life sciences, statistics, or data management.
• Minimum 6 years in clinical monitoring or trial management.
• Advanced programming and automation skills.
• Experience with CDISC governance and database design.