Manager, Statistical Programming

Job Summary

Working remotely, the full-time Manager, Statistical Programming will lead and support programming activities for clinical studies, ensuring high-quality deliverables and compliance with regulatory standards.

Key Responsibilities:

• Develop Tables, Figures, Listings (TFLs) for Clinical Study Reports (CSRs) from existing SAS programs and new outputs
• Independently program and review reports, customizing outputs according to delivery specifications
• Contribute to best practices for quality and efficiency while managing project risks and team activities

Required Qualifications:

• Bachelor's degree in computer science, statistics, or related scientific disciplines with 6 years of clinical programming experience; or a Master's degree with 8 years of experience
• Experience in Oncology/Hematology therapeutic areas and ISS & ISE
• Working knowledge of ICH and Good Clinical Practices, as well as the clinical trial process
• Strong understanding of the clinical drug development process and relevant regulatory requirements
• Ability to manage concurrent activities within a project effectively