1 to 25 of 26 Statistical Programmer Jobs in the UK

pharmaceutical clients, with the support of Cytel right behind you, you'll be at the heart of our client's innovation. As a Principal Statistical Programmer you will be dedicated to one of our global pharmaceutical clients; a company that is driving the next generation of patient treatment … this new program. Position Overview: This position reports to the Director, Biostatistics and Programming in the FSP Services business unit in Cytel. The Principal Statistical Programmer works independently with only concept level instruction and very little supervision, tracks progress, and provides expert technical support to team members. ...

Parexel is looking for a Senior Statistical (SAS) Programmer to join our FSP team in either the UK, Hungary, Poland or Serbia The Senior Statistical Programmer provides technical expertise for the conduct of clinical trials, acts as an internal subject matter expert in specific areas providing … expert advice, and works independently to support various programing activities related to the analysis and reporting of clinical study data. In addition, the Senior Statistical Programmer can fill the Statistical Programming Lead role on projects, and liaise with sponsors, Biostatistics Leads, Data Management Leads, and other functional ...

patient. We take our work personally, we do it with empathy and we're committed to making a difference.Parexel is looking for a Senior Statistical (SAS) Programmer to join our FSP team in either the UK, Hungary, Poland or SerbiaThe Senior Statistical Programmer provides technical expertise … expert advice, and works independently to support various programing activities related to the analysis and reporting of clinical study data. In addition, the Senior Statistical Programmer can fill the Statistical Programming Lead role on projects, and liaise with sponsors, Biostatistics Leads, Data Management Leads, and other functional ...

both via regularly scheduled group meetings to discuss issues, and impromptu one‐on‐one discussions between colleagues to discuss a particular topic. As a Statistical Programmer on a project – you will be working with statisticians, sponsors, the wider study team and your own team of programmers, ensuring … data and output delivered for a study meets industry, regulatory submission and quality standards. As a Statistical Programmer at Worldwide, your analytical skills and ability to both program and understand/interpret data are the keys to success, and you will have the opportunity to continually grow your ...

Principal Statistical Programmer, Sponsor Dedicated (part time or full time) Fully remote in UK or South Africa ONLY. Updated: Today Location: Remote, LND, United Kingdom Job ID: 25111920 Description Principal Statistical Programmer, Sponsor Dedicated (part time or full time) Fully remote in UK or South Africa … Uses SAS, or other software, to develop custom programming code to generate summary tables, data listings, graphs and derived datasets as specified in the statistical analysis plan and programming specifications. Works to ensure that outputs meet quality standards and project requirements. Performs validation programming and works with other programmers ...

Senior Clinical Statistical Programmer (Portfolio Development/Biometrics/Programming)The RoleCSL is looking for a Senior Programmer to take technical ownership of one or two clinical trials from first line of code to final submission package. This is a hands-on statistical programming role with … technical reference point for less experienced programmers, and a contributor to how the wider programming function does its work.· Serve as lead programmer for one or two clinical trials, interpreting protocols, SAPs, data management plans, and CRF specifications to drive study setup and analysis· Design and validate SDTM ...

Senior Clinical Statistical Programmer (Portfolio Development/Biometrics/Programming) The Role CSL is looking for a Senior Programmer to take technical ownership of one or two clinical trials from first line of code to final submission package. This is a hands‐on statistical programming role … technical reference point for less experienced programmers, and a contributor to how the wider programming function does its work. Serve as lead programmer for one or two clinical trials, interpreting protocols, SAPs, data management plans, and CRF specifications to drive study setup and analysis Design and validate SDTM ...

Senior Clinical Statistical Programmer (Portfolio Development/Biometrics/Programming) The Role CSL is looking for a Senior Programmer to take technical ownership of one or two clinical trials from first line of code to final submission package. This is a hands-on statistical programming role … technical reference point for less experienced programmers, and a contributor to how the wider programming function does its work. Serve as lead programmer for one or two clinical trials, interpreting protocols, SAPs, data management plans, and CRF specifications to drive study setup and analysis Design and validate SDTM ...

Principal Statistical Programmer will lead programming activities for one or more studies, ensuring high-quality development, validation, and delivery of complex analysis outputs. Drive technical excellence, innovation, and standards adoption while providing strategic insights into study data. Mentor junior programmers and influence programming approaches through strong technical leadership … Support sprint planning and project delivery across studies.Collaborate cross-functionally and manage data access appropriately.Support regulatory interactions and contribute to CoE activities.AccountabilitiesServe as Lead Programmer for complex or multiple studies.Ensure quality, compliance, and efficient execution of programming activities.Make data-driven decisions and proactively address risks and issues.Why You:Basic ...

Principal Statistical Programmer will lead programming activities for one or more studies, ensuring high-quality development, validation, and delivery of complex analysis outputs. Drive technical excellence, innovation, and standards adoption while providing strategic insights into study data. Mentor junior programmers and influence programming approaches through strong technical leadership … project delivery across studies. Collaborate cross-functionally and manage data access appropriately. Support regulatory interactions and contribute to CoE activities. AccountabilitiesServe as Lead Programmer for complex or multiple studies. Ensure quality, compliance, and efficient execution of programming activities. Make data-driven decisions and proactively address risks and issues. ...

that behind every dataset, every line of code, and every submission package, there's a patient waiting for a better option. As our Senior Statistical Programmer, you are one of the people who makes that happen. This isn't a role where your work disappears into a black … preparation (think NDA, BLA, MAA) — real regulatory milestones that mark pivotal moments in a medicine's journey Reviewing and shaping key planning documents like Statistical Analysis Plans (SAPs) and Data Presentation Plans, ensuring clarity and completeness before programming work begins - your input genuinely steers project direction Partnering with vendors ...

Description Principal Statistical Programmer, Sponsor Dedicated (part time or full time) Fully remote in UK or South Africa ONLY.Syneos Health is a leading fully-integrated life sciences services organization built to accelerate customer success. We partner with innovators at every point across the drug development and commercialization continuum … ResponsibilitiesUses SAS, or other software, to develop custom programming code to generate summary tables, data listings, graphs and derived datasets as specified in the statistical analysis plan and programming specifications. Works to ensure that outputs meet quality standards and project requirements. Performs validation programming and works with other programmers ...

ClinChoice is seeking a Principal Statistical Programmer Consultant to join a client-facing team in the United Kingdom. The role emphasizes leading statistical programming activities, delivering SAS programs, and ensuring SDTM/ADaM compliance in regulatory submissions. Ideal candidates have a CS or statistics degree with CDISC ...

Senior Clinical Statistical Programmer (Portfolio Development/Biometrics/Programming) The Role CSL is looking for a Senior Programmer to take technical ownership of one or two clinical trials from first line of code to final submission package. This is a hands-on statistical programming role ...

ClinChoice is seeking a Senior Statistical Programmer Consultant (Oncology) for a remote UK-based position outside IR35. The role involves delivering programming components under leadership, tackling complex clinical programming tasks, and coordinating with study teams to ensure quality and regulatory compliance. The ideal candidate has extensive CDISC experience ...

Worldwide Clinical Trials in the United Kingdom is seeking an experienced Statistical Programmer to lead programming efforts on medium to large-scale studies, ensuring CDISC compliance and high-quality outputs. You will develop and review SDTM/ADaM datasets, TFLs, and deliver analysis-ready data, collaborating with statisticians ...

Johnson & Johnson in High Wycombe, UK is seeking an Experienced Statistical Programmer to join the Data Analytics & Computational Sciences team. You will develop, verify, and document statistical programs for clinical data, supporting analysis and reporting with high quality deliverables. You will collaborate with cross-functional teams, ensure ...

Worldwide Clinical Trials is seeking a skilled Statistical Programmer to join our Global Programming team. You will develop and validate CDISC SDTM/ADaM datasets, create TFLs and listings, and contribute to submission-ready packages across multiple studies. You will review study specs, lead programming efforts on medium ...

Bristol Myers Squibb in the UK is seeking a Senior Statistical Programmer to drive programming work within our Global Biometrics & Data Sciences function, collaborating with cross-functional clinical teams and external vendors. This role offers autonomy, high-impact projects, and exposure to regulatory submissions; you will produce SDTM ...

Syneos Health in the United Kingdom is seeking a Principal Statistical Programmer to lead sponsor-dedicated programming efforts. The role supports remote work for UK or South Africa, with responsibilities across SAP-driven outputs and regulatory compliance. The successful candidate will mentor team members, ensure compliant CDISC standards ...

Plasma Inc. is seeking a Senior Clinical Statistical Programmer to own the programming for one or two trials from setup to submission, collaborating with statisticians, data managers and regulatory colleagues. You will influence study analysis structures and ensure audit-ready outputs across SDTM/ADaM datasets, TFLs ...

Seqirus in Maidenhead is seeking a Senior Clinical Statistical Programmer to take technical ownership of one or two trials from first line code to submission-ready packages. This hands-on role requires building and validating SDTM/ADaM datasets, TFLs and delivery of analysis outputs with regulatory scrutiny ...

data from multiple trials (e.g. ISS and ISE datasets). These designs and specifications are completed in accordance with common industry standards and conventions, statistical requirements and specifications, and/or clinical trial sponsor’s requirements. Generate complete and efficient analysis data models following approved dataset designs or specifications. … Perform independent validation of datasets created by other programmers or statisticians. Develop SAS programming codes and generate complete and accurate statistical output reports of trial data in well-defined formats. Develop SAS programming codes to independently validate statistical output reports of trial data generated by other programmers ...

service contract research organization providing expertise-based clinical research services to the pharmaceutical, biotechnology, and medical device industries. Everest is seeking a senior SAS Programmer to design data tabulation and analysis data models, develop robust SAS code, validate outputs, and support continuous improvement of statistical programming processes within ...

Parexel is seeking a Senior Statistical (SAS) Programmer to join our FSP team in the UK, Hungary, Poland or Serbia. The role provides technical expertise for clinical trial analysis and reporting, acting as an internal SME and supporting programming activities across study data. You will lead a global ...