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ClinChoice is seeking a Senior Statistical Programmer Consultant in the United Kingdom.

A leading clinical research organization is seeking a Senior Statistical Programmer to join their team remotely from anywhere in the UK. The role involves developing SAS programming codes, generating analysis data models, and ensuring quality in statistical reporting for clinical trials.

Senior Principal Statistical Programmer (RWE). Senior Principal Statistical Programmer. This role involves leading statistical programming for real-world data (RWD) projects and developing interactive applications to support decision-making, regulatory, and HTA submissions.

Owing to the large body of work – mostly internally funded – the team is recruiting for a Statistics and Psychometrics Lead, one entry‑level Statisticians/Psychometrician, and one Statistical Programmer to support the teams’ activities, as described below. The Statistician/Psychometrician an

A global pharmaceutical company in Greater London is seeking a Principal Statistical Programmer to lead statistical programming for clinical studies. You will coordinate programming activities, ensure compliance with industry standards, and maintain quality control of statistical analysis deliverabl

A leading clinical research organization in Greater London is seeking a Statistical Programmer to develop scoring algorithms for COA measures and provide programming support for new endpoints.

A leading pharmaceutical consulting firm in the United Kingdom is seeking a Principal Statistical Programmer. You will be responsible for generating SDTM, ADaM specifications, and overseeing CRO statistical programming deliverables.

Lead statistical programming activities as Trial Programmer for either a large/pivotal study or several studies, or act as a Lead/Program Programmer for a small to medium sized project in phase I to IV clinical studies in Novartis Global Drug Development. The Principal Statistical Programmer is resp

Senior Statistical Programmer (contract). The Senior Statistical Programmer will contribute expert programming skills to deliver accurate, regulatory-compliant clinical data outputs for Compass Pathways development programs. Reviewing of the Statistical Analysis Plan (SAP) and shells.

A leading global CRO is seeking a Senior Statistical Programmer for a permanent home-based position.

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 ad

A global clinical research services provider in Greater London is seeking a Statistical Programmer to develop scoring algorithms and collaborate on patient-centered research.

A biotechnology company is seeking a Senior Statistical Programmer for a fixed-term contract of 9 months. The ideal candidate will have extensive statistical programming experience, knowledge of regulatory submissions, and proficient skills in SAS and R.

Act as a shadow lead programmer and attend customer meetings alongside the Lead Programmer as required. We are looking for a SAS Programmer III who can also program in R with a background in working across clinical trials, ideally with experience in oncology. You will work closely with programmers,

A leading pharmaceutical company is seeking a Senior Principal Programmer who will oversee statistical programming for clinical trials.

A leading global provider of advanced analytics in London is looking for a Senior Statistical Programmer. This role involves designing data specifications, ensuring submission readiness of clinical data, and leading statistical programming activities using SAS for clinical trials.

Clinical Programmer (SCP) plays a pivotal role in supporting clinical research by developing, validating, and maintaining statistical programs and datasets. Get notified about new Statistical Programmer jobs in. Collaborating with Biostatisticians, Clinical Data Managers, and cross-functional teams,

A leading global CRO is seeking a Senior Statistical Programmer to support clinical data submissions. Candidates should have a BSc in a related field and at least 5 years of experience in clinical statistical programming.

We have an exciting opportunity for a Senior or Principal Statistical Programmer with strong SAS experience (and R exposure advantageous) to join Veramed on a permanent basis in the UK. At least 4 years’ relevant industry experience in statistical programming.

Are you an experienced statistical programmer ready to take the next step in your career? We are expanding our clinical programming team and are looking for a leader in programming, skilled in SAS, confident working with clinical trial data and CDISC standards. Support junior programmers through day

Statistical Programmer II | Leading CRO | Home Based | UK. We’re seeking several Statistical Programmer II positions to join this growing organisation remotely from the UK. You’ll support statistical programming activities across clinical trials, ensuring high‑quality and timely deliverables.

We are looking for a highly experienced senior statistical programmer who will work on clinical development programs in different therapeutic areas and participate in overseeing CRO programmers to ensure that data summaries are delivered in a consistent, high-quality manner. Statistical Programmer o

Senior Statistical Programmer 1 - UK/EU - Remote. Senior Statistical Programmer | Independent CRO | Home Based | UK |. We’re seeking elite Senior Statistical Programmers to join this growing organisation remotely from anywhere in the UK.

The Senior Statistical Programmer will be responsible for review datasets in submission ready standard format (ADaM), tables, figures, listings and submission packages. Lead and oversee the development of global tools that will increase the efficiency and capacity of the Statistical Programming grou

A leading contract research organization is seeking a Principal Statistical Programmer to provide programming leadership for complex studies. This fully home-based role requires expertise in SAS, and a background in statistical programming.

We are looking for a highly experienced senior statistical programmer who will work on clinical development programs in different therapeutic areas and oversee CRO programmers to ensure that data summaries are delivered consistently, high‑quality, and on schedule. As a Principal Statistical Progra

A leading CRO is seeking a Statistical Programmer II to join their team remotely from the UK. This role involves supporting statistical programming activities across clinical trials, developing and validating datasets, and ensuring compliance with clinical data standards.

Develop SAS programming codes to independently validate statistical output reports of trial data generated by other programmers or statisticians. Provide technical guidance and support to less experienced Statistical Programmers. Develop SAS programming codes and generate complete and accurate stati

A leading statistical consultancy in the UK is seeking a Senior or Principal Statistical Programmer to join their team. Candidates should have strong SAS experience and at least 4 years in statistical programming.

Cytel - EMEA is looking for a Principal Statistical Programmer to work on clinical development programs for a global pharmaceutical client. This role involves generating SDTM and ADaM specifications, developing SAS programs, and ensuring high-quality statistical deliverables.

World leading CRO recently awarded Best Employer have a new opportunity for a Principal Statistical Programmer to join their FSP Team. If this opportunity is of interest, please apply now with your CV as the organisation are looking to welcome the new Principal Statistical Programmer onboard as soon

Lead statistical programming activities as Trial Programmer for several studies or as Lead/ Program Programmer for a medium to large sized project in phase I to IV clinical studies in Novartis Global Development Organization. Responsible for quality control and audit readiness of all assigned statis

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