Overview
We are seeking experienced Senior and Principal Statistical Programmers to join our team in preparation for multiple upcoming projects throughout 2027. This remote role offers the opportunity to work directly with a single sponsor while benefiting from the resources and career development opportunities provided by a global CRO. The successful candidates will lead statistical programming activities across clinical trials in therapeutic areas such as Oncology, Rare Disease, or Neuroscience, collaborating closely with cross-functional teams to ensure high-quality and timely deliverables.
Responsibilities
- Serve as a lead statistical programmer for multiple studies and/or compounds.
- Lead and execute statistical programming activities from study start-up through regulatory submission.
- Ensure consistency, quality, and executional excellence across programming deliverables.
- Support programming activities for global regulatory submissions and health authority questions.
- Provide technical oversight and guidance for outsourced programming activities.
- Develop, review, and validate statistical programming deliverables, including TLFs and datasets.
- Contribute to the development and continuous improvement of SAS programming standards.
- Identify opportunities to improve programming processes and support complex study designs.
Requirements
- Strong proficiency in SAS programming within a pharmaceutical, biotechnology, or CRO environment.
- Strong understanding of CDISC standards, including SDTM and ADaM.
- 8+ years of statistical programming experience supporting clinical development.
- Experience in one or more of the following therapeutic areas: Oncology, Rare Disease, or Neuroscience.
- Hands-on experience with SDTM and ADaM specification and programming.
- Experience in clinical trial reporting and regulatory submissions.
- Bachelor or MSc in Statistics, Mathematics, or related scientific discipline is required.
- English language proficiency is essential; proficiency in French is preferred.