🛠 Tech Stack

💼 About This Role

You'll lead PK/PD statistical programming for global clinical trials, transforming complex pharmacokinetic data into analysis-ready datasets. Your work directly supports regulatory submissions and accelerates drug development.

🎯 What You'll Do

• Develop and validate SAS/R outputs like tables, listings, and figures.
• Design PK/PD analysis datasets (ADPC, ADPP, ADNCA) per CDISC standards.
• Generate and validate NCA and NONMEM datasets for PK/PD analyses.
• Serve as lead programmer, coordinating activities across multiple studies.

📋 Requirements

• 5+ years of clinical statistical programming experience.
• SAS expertise and intermediate to advanced R proficiency.
• Strong knowledge of PK/PD workflows and clinical trial designs.
• Experience with CDISC standards and regulatory requirements.

✨ Nice to Have

• Hands-on experience with NONMEM and NCA datasets.
• Acted as technical lead or mentored junior programmers.

🎁 Benefits & Perks

• 💻 Remote work flexibility.
• 📈 Career development opportunities in global clinical research.
• 🧠 Structured learning programs and technical training.
• 🌍 Large-scale global studies with high scientific impact.
• 🤝 Inclusive, science-driven work environment.

📨 Hiring Process

Estimated timeline: 2-4 weeks · AI estimate

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