At a Glance
- Tasks: Lead and support clinical trials using advanced SAS programming skills.
- Company: Join Cytel, a leader in pharmaceutical innovation with a collaborative culture.
- Benefits: Enjoy remote work, continuous training, and professional development opportunities.
- Other info: Dynamic role with opportunities to lead multiple projects and grow your career.
- Why this job: Make a real impact on patient treatment while working with cutting-edge data.
- Qualifications: 8+ years of SAS programming experience in clinical trials required.
The predicted salary is between 63000 - 77000 £ per year.
Working fully embedded within one of our pharmaceutical clients, with the support of Cytel right behind you, you'll be at the heart of our client's innovation.
As a Senior Statistical Programmer you will be dedicated to one of our global pharmaceutical clients; a company that is driving the next generation of patient treatment, where individuals are empowered to work with autonomy and ownership.
As a Senior Statistical Programmer, you will leverage your advanced SAS programming skills and proficiency in CDISC standards (SDTM & ADa M) to support or lead one or more Phase I-IV clinical trials.
This role can be performed as fully remote.
Our values We believe in applying scientific rigor to reveal the full promise inherent in data.
We believe in collaboration and invite a diversity of perspectives, drawing on a variety of talents to create a wealth of possibilities.
Here at Cytel we want our employees to succeed and we enable this success through consistent training, development and support.
Bachelor's degree in one of the following fields Statistics, Computer Science, Mathematics, etc.
At least 8 years of SAS programming working with clinical trial data in the Pharmaceutical & Biotech industry with a bachelor's degree or equivalent.
At least 6 years of related experience with a master's degree or above.
Study lead experience, preferably juggling multiple projects simultaneously preferred.
Strong SAS data manipulation, analysis and reporting skills. Strong QC / validation skills. Good ad-hoc reporting skills. Proficiency in Efficacy analysis.
Familiarity with drug development life cycle and experience with the manipulation, analysis and reporting of clinical trials' data.
xml and other submission documents.
Ability to provide quality output and deliverables, in adherence with challenging timelines.
Performing data manipulation, analysis and reporting of clinical trial data, both safety and efficacy (ISS/ISE), utilizing SAS programming Generating and validating SDTM and ADa M datasets/analysis files, and tables, listings, and figures (TLFs)Production and QC / validation programming Generating complex ad-hoc reports utilizing raw data Applying strong understanding/experience of Efficacy analysis Creating and reviewing submission documents and e CRTs Communicating with and/or responding to internal cross-functional teams and client for project specifications, status, issues or inquiries Performing lead duties when called upon Serving as team player, with a willingness to go the extra distance to get results, meet deadlines, etc.
- Being adaptable and flexible when priorities change Full time
- Posting Date: 2026-08-05
Principal SAS Programmer employer: Cytel
Cytel is an exceptional employer that empowers its employees to thrive in a collaborative and innovative environment, particularly for the role of Principal SAS Programmer. With a strong commitment to professional development and training, Cytel ensures that you have the support needed to excel in your career while working remotely with a leading global pharmaceutical client. The company values diversity of thought and encourages autonomy, making it an ideal place for those looking to make a meaningful impact in the field of clinical trials.
