🛠 Tech Stack

💼 About This Role

You'll develop and validate SAS programming deliverables to support clinical study analysis and reporting. You'll collaborate with Biostatistics and cross-functional teams to produce high-quality, compliant datasets and ensure adherence to regulatory requirements and CDISC standards. This role offers the chance to work on Phase 3 and regulatory submission projects.

🎯 What You'll Do

• Program and validate tables, listings, figures, and derived datasets using SAS.
• Develop SDTM and ADaM datasets and supporting documentation.
• Perform quality control and validation activities for programming deliverables.
• Prepare and review mapping specifications and annotated case report forms.

📋 Requirements

• Bachelor's degree in Statistics, Biostatistics, Mathematics, Computer Science, or related field
• Minimum of 10 years of relevant statistical programming experience in pharma/biotech/CRO
• Strong SAS programming skills with SDTM and ADaM experience
• Experience with Phase 3 and regulatory submission preferred

✨ Nice to Have

• Master's degree in a related field
• Knowledge of CDISC standards
• Experience with regulatory submission packages

🎁 Benefits & Perks

• 💻 Remote work flexibility
• 📋 Contract role with potential for extension
• 🏥 Health insurance options available
• 💵 Competitive hourly rate

📨 Hiring Process

Estimated timeline: 2-4 weeks · AI estimate

1. 1Recruiter Screen· 30 min
2. 2Hiring Manager Interview· 60 min
3. 3Technical Assessment· 60 min