Statistical Programmer

Our client is seeking a highly motivated and experienced Statistical Programmer (Contractor) to support clinical development programs across Phases 1â 3. This role requires a hands-on contributor with strong technical skills, a collaborative mindset, and the ability to thrive in a fast-paced biotech environment.

Weâ re looking for someone who is eager to roll up their sleeves and provide high-quality programming support across a range of clinical deliverables.

Key Responsibilities:

Develop and validate SAS programs for analysis datasets (SDTM, ADaM), tables, listings, and figures (TLFs) for clinical trials

Collaborate with biostatisticians and data managers to support statistical analysis and reporting for Phase 1â 3 trials

Ensure programming deliverables meet regulatory submission standards and internal quality guidelines

Perform quality control and validation of outputs to ensure accuracy and consistency

Contribute to the development and maintenance of programming documentation and standard operating procedures

Troubleshoot programming issues and resolve data-related problems in a timely manner

Support ad hoc analyses and data requests from clinical and regulatory teams Requirements / Qualifications:

Bachelorâ s or Masterâ s degree in Statistics, Computer Science, Mathematics, or a related field

5+ years of SAS programming experience in the biotech or pharmaceutical industry

Strong experience with CDISC standards (SDTM and ADaM) and FDA/EMA submission requirements

Proven experience working on global clinical trials across Phases 1â 3

Ability to manage competing priorities in a fast-paced, evolving environment

Detail-oriented with strong problem-solving and analytical skills

Excellent communication skills and the ability to work both independently and as part of a cross-functional team

Self-starter with a "roll-up-your-sleeves" attitude and team-oriented mindset