Statistical Programmer
ProKidney
WorldwideFully remoteContractHealthcare & Telemedicine
No salary statedPosted 23 days ago3w ago
Why we think you can apply
- Hiring model
- Open worldwide · the employer states no country restriction
- Work from
- Anywhere, the UAE included
Posted 23 days ago
About the role
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
What we look for
- Bachelor's degree in Statistics, Biostatistics, Mathematics, or Computer Science
- 10+ years of statistical programming experience
- Proficiency in SAS
- Experience with SDTM and ADaM
- Knowledge of clinical trial processes
SASSDTMADAMCDISC
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