Join to apply for the Senior Statistical Programmer FSP role at Axio Research Job Description Working fully embedded within one of our pharmaceutical clients, with the support of Cytel, you will be at the heart of our client's innovation. As a Senior Statistical Programmer, you will be dedicated to a global pharmaceutical company driving the next generation of patient treatment, where individuals are empowered to work autonomously and take ownership. This is an exciting time to be part of this new program. Position Overview 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 a 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, and tables, listings, and figures (TLFs). Produce programming for QC/validation. Generate complex ad‑hoc reports utilizing raw data. Apply strong understanding and 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. Be adaptable and flexible when priorities change.

Qualifications

Bachelor’s degree in Statistics, Computer Science, Mathematics, or a related field. At least 8 years of SAS programming experience with clinical trial data in the pharmaceutical and biotech industry; or at least 6 years of related experience with a master’s degree or above. Study lead experience, preferably juggling multiple projects simultaneously. Strong SAS data manipulation, analysis, and reporting skills. Solid experience implementing the latest CDISC SDTM/ADaM standards. Strong QC/validation skills. Good ad‑hoc reporting skills. Proficiency in efficacy analysis. Familiarity with the drug development life cycle and experience with the 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 in adherence with challenging timelines. Ability to work effectively and successfully in a globally dispersed team environment with cross‑cultural partners.

Job Info

Job Identification: 1085 Job Category: Statistical Programming – FSP Posting Date: 11/03/2025, 01:49 PM Location: 6th Floor, 9 Appold Street, London, EC2A 2AP, GB Job Schedule: Full time

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