🛠 Tech Stack

💼 About This Role

You'll lead the design of advanced SAS macros for TLF automation and clinical programming in global drug development. Your work directly enhances regulatory submission quality and efficiency. This role combines deep technical expertise with strategic influence in a GxP-regulated environment.

🎯 What You'll Do

• Design and maintain advanced, reusable SAS macros for TLF generation
• Develop enterprise-level tools for data transformation and QC
• Ensure compliance with SDLC, GxP, and 21 CFR Part 11
• Collaborate with biostatisticians and programmers on technical solutions

📋 Requirements

• 12+ years of SAS programming in pharma/biotech/CRO
• 5+ years dedicated SAS macro development with enterprise automation
• Advanced SAS/Macro proficiency for complex dynamic macros
• Deep knowledge of CDISC standards (SDTM, ADaM, Define-XML)

✨ Nice to Have

• Experience with Pinnacle 21 for CDISC validation
• Familiarity with R, Python, or Shiny
• Leadership experience in mentoring technical teams

🎁 Benefits & Perks

• 💰 Competitive compensation aligned with senior-level expertise
• 🛠️ Lead enterprise-scale automation in global clinical development
• 📚 Strong learning opportunities in advanced SAS and leadership
• 🌍 Collaborative global work with cross-functional teams
• 🚀 Career growth in technical leadership within pharma R&D

📨 Hiring Process

Estimated timeline: 2-4 weeks · AI estimate

1. 1Phone Screen· 30 min
2. 2Technical Interview· 60 min
3. 3Hiring Manager Interview· 45 min
4. 4Offer· 1 week