💼 About This Role

You'll provide statistical programming oversight for oncology clinical trials at a late-stage biotech. You'll drive regulatory submissions and ensure CDISC compliance. This role offers leadership opportunities in a high-impact team.

🎯 What You'll Do

• Oversee statistical programming resources including contractors and CROs
• Mentor future leaders in RevMed core values
• Ensure timely delivery of analysis for statistical programming deliverables
• QC documents with clinical data for accuracy
• Manage timelines and vendors for submission-related activities

📋 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 experience supporting clinical trial analysis datasets and outputs

✨ Nice to Have

• Oncology clinical trial experience
• Strong leadership and teamwork track record
• Innovative approaches in a collaborative environment

🎁 Benefits & Perks

• 💰 Base salary $164k-$205k
• 📈 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