Statistical Programmer

ProKidney

Completely RemoteContractHealthcare & Telemedicine
Posted Yesterday

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

Skills & tools

SASSDTMADAMCDISC

What the team is looking for

Use this list as a quick fit check before you apply.

  1. 01Bachelor's degree in Statistics, Biostatistics, Mathematics, or Computer Science
  2. 0210+ years of statistical programming experience
  3. 03Proficiency in SAS
  4. 04Experience with SDTM and ADaM
  5. 05Knowledge of clinical trial processes
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