🛠 Tech Stack

💼 About This Role

You'll lead statistical programming projects for clinical trials and regulatory submissions, ensuring high-quality outputs that drive drug development decisions. You will oversee complex SAS programming, coordinate cross-functional teams, and mentor junior programmers in a remote, collaborative environment.

🎯 What You'll Do

• Lead statistical programming project teams to deliver analysis datasets and outputs on time
• Manage project resources, timelines, budgets, and study-level metrics across multiple initiatives
• Collaborate with statisticians and clients to review analysis plans and implement requirements
• Develop, review, and maintain analysis dataset specifications and complex SAS programs
• Produce and validate statistical outputs including SDTM/ADaM datasets and regulatory documentation

📋 Requirements

• Bachelor's degree or equivalent in a relevant field
• 10+ years of SAS programming experience, including at least 7 years in pharmaceutical or clinical research industry
• Strong expertise in SAS/Base, SAS Macro programming, and CDISC standards (SDTM, ADaM)
• Proven ability to lead programming teams and manage multiple concurrent projects
• Experience with regulatory deliverables and technical documentation

✨ Nice to Have

• Experience with DEFINE.xml and Reviewer's Guides
• Familiarity with R or Python for statistical programming
• Knowledge of real-world evidence generation

🎁 Benefits & Perks

• 🏖️ Fully remote work across the United States
• 💰 Competitive salary with 401(k) company match
• 🏥 Comprehensive medical, dental, vision insurance
• 🎓 Tuition reimbursement and career development opportunities
• 📅 Flexible PTO and paid holidays

📨 Hiring Process

Estimated timeline: 2-4 weeks · AI estimate

1. 1Recruiter call· 30 min
2. 2Technical interview· 60 min
3. 3Final interview with management· 60 min