🛠 Tech Stack

💼 About This Role

You'll lead statistical programming activities for Phase I–IV clinical studies in a global, collaborative environment. Your work directly supports regulatory submissions and clinical reporting with high-quality datasets and analysis outputs. This role offers a chance to shape processes and mentor junior programmers while working on impactful global programs.

🎯 What You'll Do

• Lead statistical programming across Phase I–IV studies
• Develop SDTM and ADaM datasets with CDISC standards
• Program and validate SAS outputs for TLFs
• Mentor junior programmers and support knowledge sharing

📋 Requirements

• Bachelor's in Statistics, Computer Science, or related field
• 4+ years in statistical programming in pharma or CRO
• Strong expertise in SAS programming
• Knowledge of CDISC standards (SDTM, ADaM)

✨ Nice to Have

• Knowledge of R or Python
• Regulatory submission package experience
• Mentoring experience

🎁 Benefits & Perks

• 💰 Competitive compensation
• 🏥 Health and wellness benefits
• 📚 Professional development opportunities
• 🌍 Global clinical development exposure
• 🔄 Flexible/hybrid work arrangements

📨 Hiring Process

Estimated timeline: 2-4 weeks · AI estimate

1. 1Recruiter call· 30 min
2. 2Technical interview· 60 min
3. 3Hiring manager interview· 45 min