Associate Director, Evidence Generation Statistical Programming - Remote

Overview

The Associate Director of Evidence Generation Statistical Programming will provide statistical programming technical support to project teams, improving programming efficiency and ensuring compliance with regulatory standards.

In Short

• Support project leads on outsourced projects.
• Perform programmatic reviews of SDTM and ADaM datasets.
• Develop programming standards and templates.
• Create and maintain programming macros and tools.
• Assist in regulatory submissions and responses.
• Evaluate and enhance the computing environment system.
• Provide hands-on statistical programming support.
• Contribute to CRF and SDTM standard development.
• Lead macro or tool development efforts.
• Ensure quality and integrity of analysis datasets.

Requirements

• Bachelor's or Master's Degree in a science or technical field preferred.
• 10+ years experience in the pharmaceutical industry or CROs.
• Advanced knowledge of SAS programming.
• Experience with CDISC SDTM and ADaM.
• Solid background in applied statistics.
• Knowledge of drug development phases.
• Experience with advanced statistical methods using SAS and R.
• Strong understanding of database structures.
• Ability to support regulatory submissions.
• Proven experience in programming support for clinical trials.

Benefits

• Collaborative working environment.
• Focus on personal accountability and results.
• Training and development opportunities.
• Valued individual contributions.
• Open communication culture.