🛠 Tech Stack

💼 About This Role

You'll lead statistical programming for oncology clinical trials, providing hands-on SAS support and oversight of regulatory submissions. You'll also manage vendors and timelines while ensuring CDISC compliance.

🎯 What You'll Do

• Provide SAS programming support and guidance to programming team.
• Oversee regulatory submissions and audits.
• Manage timelines and vendor deliverables.
• Lead development of clinical study datasets and outputs.

📋 Requirements

• 14+ years of statistical programming experience in oncology trials.
• BS/BA degree in relevant field.
• Proficiency in SAS programming for analysis datasets and TLFs.
• Experience leading programming contractors and vendors.

✨ Nice to Have

• Small to mid-sized biotech/pharma experience.
• Experience developing SOPs and guidance documents.
• Strong leadership and teamwork record.

🎁 Benefits & Perks

• 💰 Competitive cash compensation
• 📈 Robust equity awards
• 🏥 Strong benefits
• 📚 Significant learning and development opportunities

📨 Hiring Process

Estimated timeline: 3-5 weeks · AI estimate

1. 1Application Review· 1-2 weeks
2. 2Phone Screen· 30 min
3. 3Virtual Interview· 1 hour
4. 4On-site Interview· 4 hours
5. 5Offer· 1 week