💼 About This Role

You'll provide statistical programming oversight for oncology clinical trials at a late-stage biotech. You'll ensure quality and timely delivery of analysis datasets and regulatory submissions. This role offers the chance to mentor future leaders and shape statistical programming processes.

🎯 What You'll Do

• Oversee statistical programming resources including contractors and CROs
• Ensure accuracy of clinical trial results via QC of documents
• Manage timelines and vendors for submission-related deliverables
• Provide programming support for Dose Committee meetings and regulatory submissions

📋 Requirements

• 10-14 years of statistical programming experience in biotech/pharma
• BS/BA degree or relevant qualification
• Experience with CDISC standards (SDTM, ADaM, define.xml)
• Direct programming support for early or late-phase clinical trials

✨ Nice to Have

• Experience with oncology clinical trials
• Demonstrated leadership and teamwork skills

🎁 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 phone screen· 30 min
2. 2Technical interview· 60 min
3. 3Hiring manager interview· 45 min