Senior Statistical Programmer/Analyst Consultant

Key Responsibilities:

• Supports programming deliveries of a clinical study or project, ensuring high-quality and compliance with standards.
• Contributes to best practices to improve quality, efficiency, and effectiveness within the function.
• Works proactively with study team members and communicates and escalates risks appropriately.

Education and Experience:

• Bachelor’s or Master’s degree in computer science, statistics, or related disciplines with 5-6 years of clinical programming (CDISC) experience.
• Requires Oncology TA experience and a strong understanding of the clinical drug development process.
• Demonstrated strong communication and coordination skills to influence stakeholders and manage activities.

Company Ethos:

• Mission focuses on accelerating drug and device development for a healthier world, with employees as the most valuable asset.
• Culture emphasizes diversity, inclusivity, and continuous training to maintain high-quality personnel and low turnover rates.
• Operates as an equal opportunity employer with a global team across the Americas, Europe, and Asia-Pacific.