1437# Senior/Principal R Programmer Consultant (Remote)

Bachelor’s or Master’s degree in Computer Science, Statistics, Life Sciences, or related field. 5+ years of experience in clinical programming within pharmaceutical, biotech, or CRO environments. Expert-level programming skills in SAS (Base, Macro, SQL). Strong experience with R (including packages like tidyverse, haven, ggplot2). Proficiency in developing dashboards and reports using Power BI (including DAX and Power Query). Solid knowledge of CDISC SDTM and ADaM standards. Familiarity with regulatory submission requirements and documentation for FDA/EMA. Strong analytical, problem-solving, and organizational skills. Ability to manage multiple priorities and work collaboratively across cross-functional teams.

Develop, validate, and maintain analysis datasets (SDTM/ADaM), Tables, Listings, and Figures (TLFs) using SAS and R. Design and implement data visualization dashboards in Power BI. Collaborate with biostatistics, data management, clinical operations, and other functional teams. Contribute to the development, refinement, and documentation of standard macros, templates, and programming processes. Participate in the review of study protocols, CRFs, and statistical analysis plans (SAPs). Ensure compliance with CDISC standards (SDTM, ADaM) and applicable regulatory requirements (e.g., FDA, EMA). Provide technical mentorship and support to junior programmers. Lead or contribute to programming activities in support of regulatory submissions.