🛠 Tech Stack

💼 About This Role

You'll lead statistical programming for oncology clinical trials, ensuring CDISC compliance and regulatory submissions. Your work directly impacts the development of novel RAS-targeted therapies for cancer patients.

🎯 What You'll Do

• Lead programming support for clinical studies and regulatory submissions.
• Ensure CDISC-compliant datasets (SDTM, ADaM) and related documentation.
• Oversee vendor and timeline management for programming deliverables.
• Collaborate cross-functionally on exploratory analyses and publications.

📋 Requirements

• 14+ years statistical programming in oncology trials.
• SAS proficiency for dataset and TFL production.
• Leadership experience managing contractors and vendors.
• CDISC standards knowledge (SDTM, ADaM) for submissions.

✨ Nice to Have

• Experience in small to mid-sized biotech/pharma.
• Contributions to SOPs and guidance documents.
• Strong collaborative and innovative mindset.

🎁 Benefits & Perks

• 💰 Competitive base pay ($186k-$233k).
• 📈 Equity awards included in 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· 45 min
3. 3Technical Interview· 60 min