Description

You will lead statistical programming tasks for clinical trial data, focusing on safety and efficacy reporting.

Responsibilities

• Perform hands-on statistical programming to create, validate, and maintain analysis files, tables, listings, and figures.
• Lead small team projects and sub-team tasks with minimal supervision.
• Implement CDISC SDTM, ADaM, and Define standards.
• Provide technical and process-related guidance to study programmers and assist the Study Lead Programmer.
• Collaborate with cross-functional study team members in a globally dispersed environment.
• Develop specification documents and maintain associated tracking and validation documentation.

Required Skills

• 5+ years of statistical programming experience in a clinical development environment.
• Advanced SAS data manipulation, analysis, and reporting skills.
• Expertise in CDISC SDTM implementation.
• Working knowledge of CDISC ADaM and Define standards.
• Experience with the drug development life cycle and clinical trial data.
• Ability to execute complex programming tasks under challenging timelines.
• Strong oral and written English communication skills.
• Degree in Statistics, Mathematics, Computer Science, Life Sciences, or a related scientific subject.

Key Skills

Education

Any Graduate