Senior Statistical Programmer Working fully embedded within one of our pharmaceutical clients, you will be at the heart of our client's innovation. As a Senior Statistical Programmer you will leverage your advanced SAS programming skills and proficiency in CDISC standards (SDTM & ADaM) to support or lead one or more Phase I-IV clinical trials. This role can be performed fully remote. Our Values

We believe in applying scientific rigor to reveal the full promise inherent in data. We nurture intellectual curiosity and encourage everyone to approach new challenges with enthusiasm and the desire for discovery. We believe in collaboration and invite a diversity of perspectives, drawing on a variety of talents to create a wealth of possibilities. We prize innovation and seek intelligent solutions using leading-edge technology.

Responsibilities

Perform data manipulation, analysis and reporting of clinical trial data, both safety and efficacy (ISS/ISE), utilizing SAS programming. Generate and validate SDTM and ADaM datasets/analysis files, tables, listings, and figures (TLFs). Perform production and QC/validation programming. Generate complex ad-hoc reports utilizing raw data. Apply strong understanding/experience of efficacy analysis. Create and review submission documents and eCRTs. Communicate with and/or respond to internal cross‑functional teams and client for project specifications, status, issues or inquiries. Perform lead duties when called upon. Serve as a team player, with a willingness to go the extra distance to get results and meet deadlines. Adapt and be flexible when priorities change.

Qualifications

Bachelor’s degree in Statistics, Computer Science, Mathematics, or related field. At least 8 years of SAS programming experience with clinical trial data in the pharmaceutical/bio‑tech industry (6 years with a master’s degree or above). Study lead experience; preference for candidates who can juggle multiple projects simultaneously. Strong SAS data manipulation, analysis, and reporting skills. Solid experience implementing the latest CDISC SDTM/ADaM standards. Strong QC/validation skills. Proficiency in ad‑hoc reporting. Experience in efficacy analysis. Familiarity with the drug development life cycle and experience with manipulation, analysis, and reporting of clinical trials’ data. Submission experience utilizing define.xml and other submission documents. Experience supporting immunology, respiratory, or oncology studies is a plus. Excellent analytical and troubleshooting skills. Ability to provide quality output and deliverables within challenging timelines. Ability to work effectively in a globally dispersed, cross‑cultural team environment.

#J-18808-Ljbffr