Statistical Programming Manager

Job Summary

Providing lead oversight for complex clinical projects, the full-time Statistical Programming Manager will manage and mentor a team of Statistical Programmers, ensuring timely delivery of programming and regulatory submission deliverables while contributing to best practices in a remote work environment.

Key responsibilities

• Oversees statistical programming support for multiple clinical research study projects or teams
• Manages staff, including training, mentoring, and performance management, while ensuring project resources are effectively allocated
• Implements improvements in programming documentation, standardization, and best practices within the department

Required qualifications

• Bachelor's degree with 6 years or master's/doctoral degree with 4 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 a clinical research team
• Strong statistical programming skills in SAS; familiarity with R or Python is beneficial
• Ability to manage multiple tasks and priorities effectively while working independently