Senior Statistical Programmer FSP

Salary: £65,000 - 105,000 per year

Requirements:

• Bachelors degree in Statistics, Computer Science, Mathematics, or a related field, or equivalent.
• At least 8 years of SAS programming experience working with clinical trial data in the pharmaceutical or biotech industry with a bachelors degree, or at least 6 years of related experience with a masters degree or above.
• Study lead experience; experience managing multiple projects simultaneously is preferred.
• Strong SAS data manipulation, analysis, and reporting skills.
• Solid experience implementing current CDISC SDTM and ADaM standards.
• Strong quality control and validation skills.
• Good ad hoc reporting skills.
• Proficiency in efficacy analysis.
• Familiarity with the drug development life cycle and experience manipulating, analyzing, and reporting clinical trial data.
• Experience with submissions using define.xml and other submission documents.
• Experience supporting immunology, respiratory, or oncology studies is a plus.
• Excellent analytical and troubleshooting skills.
• Ability to deliver quality output within challenging timelines.
• Ability to work effectively in a globally dispersed team with cross-cultural partners.

Responsibilities:

• Perform data manipulation, analysis, and reporting for clinical trial data, including safety and efficacy (ISS/ISE), using SAS programming.
• Generate and validate SDTM and ADaM datasets and analysis files, as well as tables, listings, and figures (TLFs).
• Perform production and quality control or validation programming.
• Generate complex ad hoc reports using raw data.
• Apply a strong understanding of efficacy analysis.
• Create and review submission documents and eCRTs.
• Communicate with and respond to internal cross-functional teams and our client about project specifications, status, issues, and inquiries.
• Perform lead duties when needed.
• Collaborate as a team player, adapt when priorities change, and work to achieve results and meet deadlines.

Technologies:

• Embedded
• Support
• SAS
• XML
• C++

More:

We offer a senior statistical programming role dedicated to one of our global pharmaceutical clients, working fully embedded with the client and supported by Cytel. Our client is advancing the next generation of patient treatment and empowers people to work with autonomy and ownership. The role supports or leads Phase I–IV clinical trials and can be performed fully remotely on a full-time basis. At Cytel, we value scientific rigor, intellectual curiosity, collaboration, diverse perspectives, and innovation. We support employee success through consistent training, development, and support.

last updated 40 week of 2026