Principal Statistical Programming Consultant (EU)

Responsibilities

• Perform statistical programming activities for clinical trials, including early-phase projects, indications, and publications
• Lead at least one study team, providing technical and domain expertise
• Manage and mentor a small team of 2–4 programmers (if required)
• Develop and validate SAS analysis datasets, tables, listings, and figures (TLFs) based on specifications
• Create programs for graphs and tables used in
• Clinical Study Reports (CSRs)
• Safety reports
• Efficacy reports
• Work on data migration from legacy datasets to standards such as CDISC or client-specific formats
• Read, interpret, and implement program specification documents

Languages

Required

• Statistics

Nice to have

• Strong analytical and problem-solving skills
• Excellent communication skills (written and verbal)
• Leadership and mentoring capabilities

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