🛠 Tech Stack

💼 About This Role

You'll work with study teams to design early/late-stage protocols, draft statistical analysis plans, and perform analyses for regulatory submissions. You'll support submission activities including integrated summaries of safety and efficacy. This role offers the security of a global CRO with direct client engagement in a fully remote position.

🎯 What You'll Do

• Contribute to protocol design and development for early/late-stage studies
• Write statistical analysis plans and perform analyses for interim/final reports
• Support regulatory submission activities including integrated summaries
• Collaborate with Statistical Programmers and Data Managers on deliverables

📋 Requirements

• MS or PhD in Statistics or Biostatistics
• PhD +4 years or MS +9 years clinical trial experience in biotech or pharma
• Hands-on Phase I/II/III clinical trial experience
• Proficient in SAS programming

✨ Nice to Have

• Excellence in R programming
• Experience with regulatory submissions in US, Europe, Japan, or Rest of World

🎁 Benefits & Perks

• 🛡️ Outside IR35 contracting status
• 🌍 Fully remote within UK
• 📈 Career development opportunities within global CRO
• 🤝 Supportive culture with low turnover

📨 Hiring Process

Estimated timeline: 1-2 weeks · AI estimate

1. 1Submit CV· immediate
2. 2Phone interview· 30-45 min