🛠 Tech Stack

💼 About This Role

You'll lead statistical programming for oncology clinical trials at a late-stage biotech. Your core impact is ensuring CDISC-compliant datasets and regulatory submissions. This role offers hands-on programming and vendor oversight.

🎯 What You'll Do

• Provide SAS programming support and guidance to programming team.
• Oversee programming deliverables for regulatory submissions and audits.
• Manage timelines and vendors for submission-related activities.
• Perform hands-on programming for in-house presentations and analyses.

📋 Requirements

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

✨ Nice to Have

• Strong leadership and teamwork track record.
• Experience in small to mid-sized biotech/pharma.
• Collaboration on development of SOPs and guidance documents.

🎁 Benefits & Perks

• 💰 Competitive base pay salary range $186,000-$233,000.
• 📈 Equity awards as part of total rewards.
• 🏥 Strong benefits package.
• 📚 Learning and development opportunities.

📨 Hiring Process

Estimated timeline: 2-4 weeks · AI estimate

1. 1Recruiter Screen· 30 min
2. 2Hiring Manager Interview· 60 min
3. 3Technical Interview· 60 min