🛠 Tech Stack

💼 About This Role

You'll lead statistical programming for clinical trials at a global CRO. You'll program and validate datasets and oversee CRO deliverables to ensure high-quality submissions. This permanent role offers the stability of a sponsor and career growth of a CRO.

🎯 What You'll Do

• Program and validate derived datasets, tables, figures, listings.
• Process data from external sources and perform ad hoc analyses.
• Oversee programming deliverables from CROs.
• Contribute to CDISC-compliant submissions and Define packages.

📋 Requirements

• BS with 5+ years or MS with 3+ years statistical programming in pharma.
• Working knowledge of SAS and its components.
• Proficiency in R programming for clinical trials.
• Strong SAS Macro language skills.

✨ Nice to Have

• Experience with data integrations (ISS and ISE).
• Knowledge of drug development process.

🎁 Benefits & Perks

• 🌍 Remote work flexibility.
• 🏥 Comprehensive health coverage.
• 📈 Career growth opportunities within a global CRO.
• 🎓 Continuous training and professional development.
• 🤝 Equal opportunity inclusive culture.

📨 Hiring Process

Estimated timeline: 2-4 weeks · AI estimate

1. 1Phone Interview· 30 min
2. 2Technical Interview· 60 min
3. 3Hiring Manager Interview· 45 min