🛠 Tech Stack

💼 About This Role

You'll provide senior statistical leadership for global clinical trials, ensuring robust study design and regulatory submissions. Your work will directly shape the credibility of innovative therapies. Join a collaborative team driving high-impact drug development.

🎯 What You'll Do

• Serve as study biostatistician across Phase I-IV programs
• Lead development of Statistical Analysis Plans and TFL shells
• Oversee ADaM datasets and TFL output generation
• Provide statistical input for regulatory submissions and eCTD

📋 Requirements

• Ph.D. or M.S. in Biostatistics, Statistics, or quantitative field
• 10+ years (Ph.D.) or 15+ years (M.S.) pharmaceutical R&D experience
• Proficiency in SAS and R
• Strong understanding of clinical development across Phase I–IV

✨ Nice to Have

• Experience with NDA/BLA submissions and eCTD filings
• Oncology or dermatology clinical development exposure

🎁 Benefits & Perks

• 💰 Competitive compensation aligned with senior pharma roles
• 🌍 Flexible remote or hybrid working arrangement
• 📚 Professional growth and continuous development opportunities
• 🧬 High-impact global clinical programs

📨 Hiring Process

Estimated timeline: 2-4 weeks · AI estimate

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