🛠 Tech Stack

💼 About This Role

You'll provide statistical programming oversight for early to late-phase oncology clinical trials at a late-stage biotech company. Your work directly supports regulatory submissions and ensures accuracy of clinical trial results for internal and external audiences.

🎯 What You'll Do

• Provide technical oversight of statistical programming resources including contractors and CROs
• Ensure quality and timely delivery of analysis for statistical programming deliverables
• Ensure accuracy of clinical trial results for regulatory and academic audiences via QC
• Program deliverables for Dose Committee meetings, Investigator Brochures, and submissions

📋 Requirements

• 10-14 years of Statistical Programming experience in biotech/pharma
• BS/BA degree or equivalent relevant qualification
• Direct experience producing/verifying analysis datasets, tables, listings, figures for clinical trials
• Ability to multi-task and prioritize in a cross-functional team

✨ Nice to Have

• Early or late-stage oncology clinical trial experience
• Strong leadership and teamwork record

🎁 Benefits & Perks

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

📨 Hiring Process

Estimated timeline: 2-4 weeks · AI estimate

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