Statistical Programmer

Remotedxb; Dubai; On-site; AED 300,000 - 600,000; Full time

Job summary

Remotedxb in Dubai, UAE seeks a Senior Statistical Programmer to lead programming for clinical studies. You will design, validate SDTM/ADaM datasets, and produce tables, listings and figures, ensuring audit-ready documentation in a deadline-driven setting.

Strong SAS skills and regulatory knowledge are essential, with the ability to work independently and collaborate with cross-functional teams to resolve data issues and file submissions.

Qualifications

• Bachelor's degree in Statistics, Biostatistics, Mathematics, Computer Science, or a related field.
• Minimum of 10 years of relevant statistical programming experience in pharmaceutical, biotechnology, or CRO industry.
• Strong SAS programming skills.
• Experience developing SDTM, ADaM, tables, listings, and figures.
• Strong knowledge of clinical trial processes and regulatory requirements.
• Ability to work independently in a deadline-driven environment.

Responsibilities

• Program and validate tables, listings, figures, and derived datasets using SAS
• Develop SDTM and ADaM specs, datasets, and supporting documentation
• Prepare and review mapping specifications, annotated case report forms (aCRF), and submission files
• Perform quality control and validation activities for all programming deliverables
• Collaborate with study team members to resolve data and output issues
• Maintain complete, accurate, and audit-ready programming documentation
• Communicate project status, risks, and timeline impacts to stakeholders

Skills

Statistical programming

Independent worker

Communication

Education

Bachelor's degree in Statistics/Biostatistics/Mathematics/Computer Science

Master's degree (preferred)

Tools

SAS

SDTM/ADaM

Job description

Responsibilities

• Program and validate tables, listings, figures, and derived datasets using SAS
• Develop SDTM and ADaM specs, datasets, and supporting documentation
• Prepare and review mapping specifications, annotated case report forms (aCRF), and submission files
• Perform quality control and validation activities for all programming deliverables
• Collaborate with study team members to resolve data and output issues
• Maintain complete, accurate, and audit-ready programming documentation
• Communicate project status, risks, and timeline impacts to stakeholders

Requirements

• Bachelor's degree in Statistics, Biostatistics, Mathematics, Computer Science, or a related field
• Minimum of 10 years of relevant statistical programming experience in pharmaceutical, biotechnology, or CRO industry
• Strong SAS programming skills
• Experience developing SDTM, ADaM, tables, listings, and figures
• Strong knowledge of clinical trial processes and regulatory requirements
• Ability to work independently in a deadline-driven environment

Preferred Qualifications

• Master's degree in a relevant field
• Phase 3 and regulatory submission experience