🛠 Tech Stack

💼 About This Role

You'll lead statistical programming activities for clinical trials, ensuring high-quality SDTM and ADaM datasets and TLF outputs. You'll mentor junior programmers and collaborate with biostatisticians to deliver regulatory-compliant submissions.

🎯 What You'll Do

• Develop SAS programs for SDTM, ADaM, and TLF outputs
• Lead programming across multiple clinical studies
• Validate datasets and resolve discrepancies with biostatisticians
• Ensure compliance with CDISC standards and regulatory guidelines

📋 Requirements

• 5+ years of clinical SAS programming experience in pharma/CRO
• Strong expertise in Base SAS, SAS Macros, ADaM, and TLF
• Solid understanding of SDTM and CDISC standards
• Experience in oncology studies and ISS/ISE deliverables

✨ Nice to Have

• Experience with R programming
• Familiarity with FDA/EMA/ICH submission requirements
• Immediate availability

🎁 Benefits & Perks

• 💰 Competitive compensation aligned with experience
• 🏥 Health and wellness benefits
• 🌍 Global high-impact projects in clinical development
• 📚 Career development and mentoring
• 🔄 Flexible work arrangements

📨 Hiring Process

Estimated timeline: 2-4 weeks · AI estimate

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