Manager 2, Statistical Programming

📋 Description

• Lead statistical programming activities for Phase I–IV studies across therapeutic areas.
• Plan, execute, and monitor programming deliverables.
• Develop and maintain programming documentation per standards.
• Create/review CDISC SDTM and ADaM specs.
• Develop SAS programs for SDTM/ADaM datasets and reports.
• Mentor junior programmers and support regulatory submissions.

🎯 Requirements

• Bachelor's degree or higher in Statistics, CS, Mathematics, Engineering, Life Sciences, or related.
• 4+ years of clinical data programming in biotech/pharma/CRO/healthcare.
• Strong SAS programming in clinical trial data environments.
• Knowledge of R or Python is an advantage.
• Experience with regulatory submissions and CDISC standards (NDA/ANDA).
• Excellent analytical, communication, and ability to work independently with global teams.

🎁 Benefits

• Remote or hybrid work flexibility within India.
• Growth through technical leadership and mentoring responsibilities.
• Global collaboration with international teams across clinical research functions.
• Exposure to advanced statistical programming practices and regulatory processes.
• Competitive compensation and benefits.