Statistical Programming Manager

Job Summary

Providing oversight for complex clinical projects, the full-time Statistical Programming Manager will lead statistical programming efforts, manage a team of Statistical Programmers, and ensure timely delivery of programming and regulatory submission deliverables in a remote environment.

Key responsibilities

• Oversee statistical programming support for multiple clinical research study projects or teams
• Manage and mentor Statistical Programmers, ensuring high-quality programming deliverables and compliance with regulatory standards
• Identify and implement improvements in programming documentation, specifications, and standardization

Required qualifications

• Bachelor's or advanced degree with 10+ years of statistical programming experience in a Pharmaceutical/CRO environment
• Understanding of GCP principles and regulatory standards (FDA, EMA, ICH) in Clinical Research
• Proven leadership experience in managing clinical research teams
• Strong statistical programming skills in SAS, with familiarity in R or Python considered beneficial
• Excellent organizational and multitasking abilities, with strong decision-making skills