SAS Clinical Consultant

SDTM Clinical SAS Programmer, Onsite We have an immediate need for an experienced SDTM Clinical SAS Programmer with strong expertise in SDTM, Clinical SAS, and clinical trial data programming to support regulatory-compliant clinical data processing and submission activities. This is an Onsite position based in Upper Gwynedd, PA for a candidate with deep experience in SAS Programming, SAS Macros, CDISC Standards, SDTM/ADaM, FDA/ICH Guidelines, and clinical trial environments. The ideal candidate

The Director, Statistical Programming provides leadership and expertise in driving the development and maintenance of the CSL statistical programming capabilities which is required to meet regulatory obligations. Manages a team of programmers supporting clinical trial and integrated analyses, annual reporting, regulatory responses, publications, HTA requests and other purposes as needed within one or more therapeutic areas. The individual will work closely with the Senior Director, Clinical and

DUTIES: Proficient to write SAS codes to produce CDISC complaint datasets. Create statistical analysis outputs to be used in support of final reports, abstracts, posters, manuscripts, adhocs and other clinical publications. Write QC SAS programs for Dataset, Tables, Listings, and Figures following the departmental QC procedures and good programming practices. Write programs for ISS, ISE and pooled datasets. Revise programs for corrections, enhancements, or system environment changes. Proficient

CSL\'s R&D organization is accelerating innovation to deliver greater impact for patients. With a project-led structure and a focus on collaboration, we?re building a future-ready team that thrives in dynamic biotech ecosystems. Joining CSL now means being part of an agile team committed to developing therapies that make a meaningful difference worldwide. Could you be our next Associate Director, Programming (Macros & Automation)? The job is in our Waltham MA, King of Prussia PA or Glattbrugg S