Overview
Statistical Programmer 1 provides statistical programming support for clinical trial projects, focused on SAS programming, validation, reporting, and DM listings.
What you'll do
- Develop, validate, and maintain SAS programs and outputs for clinical trial data management, analysis, and reporting.
- Develop and maintain data transfer programs according to client specifications and project requirements.
- Develop and maintain DM SAS listings per client specifications and study standards.
- Review draft and final production outputs to ensure quality, accuracy, and consistency.
- Take ownership of the quality and integrity of assigned deliverables.
- Collaborate with cross-functional teams including Clinical Data Management, Statistical Programming, and other stakeholders.
- Prioritize and manage multiple studies and tasks in a fast-paced environment while meeting timelines.
What you'll need
- Bachelor’s degree in computer science, Life Sciences, Mathematics, Statistics, or a related discipline.
- Relevant and equivalent experience may be considered in lieu of education requirements.
- 1 to 3 years of SAS programming experience in the CRO or Pharmaceutical Industry.
- Solid understanding of programming fundamentals and program development principles.
- Mandatory experience in developing and maintaining vendor data programs.
- English required for speaking, writing, and reading.
Details
- Work environment: Office environment (Hybrid).
Read the full description and apply on the company’s own careers page.
