1 to 25 of 185 Senior Statistical Programmer Jobs

Senior Statistical Programmer Exciting role in cutting-edge research, working with some of the most distinguished pharma companies in the UK and internationally. CRO Solutions is looking for a Senior Statistical Programmer to work within our growing multidisciplinary Biometrics team. The role can either be remote-based with occasional visits to our Salford Quays … office or office-based. CRO Solutions are reinventing the way we perform statistical analysis, how we track our studies, how we define our internal standards and how we create our datasets and outputs. The candidate must have strong SAS knowledge, 2 years Lead Statistical Programmer experience and a strong working knowledge of the CDISC standards. Working on … but candidates with suitable experience are considered. The role involves defining our internal standards, leading the programming elements of a study, liaising with the Statistics group, and shaping the Statistical Programming department. Later opportunities could include mentoring, cross functional process development, standard macro development. The Role: Develop and Implement Standards : Adapt and embed CDISC standards into our internal processes More ❯

Join to apply for the Senior Principal Statistical Programmer role at Novartis We are seeking a Senior Principal Statistical Programmer with expertise in HTA, RWE, HEOR, and Pricing and Reimbursement activities. This role involves providing statistical programming solutions to HTA challenges, collaborating closely with International Value & Access and HEOR teams to optimize processes … for Joint Clinical Assessment in Europe, ensuring high-quality deliverables. The Senior Principal Statistical Programmer will oversee all statistical programming aspects of multiple studies or projects, acting as a strategic partner to ensure efficient execution of drug development plans with high-quality, timely deliverables. Responsibilities include ensuring compliance with project standards and regulatory guidelines, overseeing programming … quality, and leading process improvements. Key Responsibilities Lead statistical programming activities for medium to large projects across clinical phases I to IV. Coordinate activities of internal and external programmers, making strategic programming decisions. Possibly serve as a functional manager, supervising and advising programmers. Collaborate with cross-functional teams on deliverables, timelines, scope, and resources. Review data collection forms, data More ❯

Get AI-powered advice on this job and more exclusive features. Senior Statistical Programmer | Independent CRO | Home Based | UK | Join a fast-growing, independent CRO providing a broad range of expertise-based clinical research services to worldwide pharmaceutical, biotechnology, and medical device industries Renowned for its high-quality deliverables, exceptional customer service, and flexibility in meeting clients … growing organisation offers a flexible, dynamic, and entrepreneurial culture. With ongoing growth and exciting career opportunities, it’s the perfect place to advance your career. We’re seeking elite Senior Statistical Programmers to join this growing organisation remotely from anywhere in the UK. What you will be doing: You’ll lead statistical programming projects, ensuring high-quality … SOPs. What you will need: A Bachelor’s degree in Statistics, Biostatistics or Computer Sciences + Masters or PH.D in Statistics is essential. 6 years’ experience in clinical trial statistical programming. Excellent knowledge of SAS essential with R advantageous. Good working knowledge of data structures e.g. CDISC, SDTM, ADaM, Comprehension of clinical data standards (CDISC), TLFs, and submission guidelines. More ❯

Job Description Summary We are in search of a Senior Principal Statistical Programmer, with expertise in HTA and Pricing and Reimbursement activities. This role offers the chance to provide statistical programming solutions to HTA problems. The successful candidate will work closely with International Value & Access and HEOR teams to shape ways of working for Joint Clinical … Assessment in Europe to ensure high-quality deliverables. The Senior Principal Statistical Programmer will be responsible for all statistical programming aspects of several studies, a medium to large sized project or project-level activities. Acts as a key collaborator and strategic partner in ensuring that drug-development plans are executed efficiently with timely and high-quality … deliverables. Complies with project/study standards and specifications following internal and regulatory guidelines. Oversees programming style, quality of statistical reporting & compliance with timelines. Job Description Key requirements Lead statistical programming activities for a medium to large sized project in phase I to IV clinical studies in Novartis Global Development Organization. Co-ordinate activities of programmers either internally More ❯

We are in search of a Senior Principal Statistical Programmer, with expertise in HTA and Pricing and Reimbursement activities. This role offers the chance to provide statistical programming solutions to HTA problems. The successful candidate will work closely with International Value & Access and HEOR teams to shape ways of working for Joint Clinical Assessment in Europe … to ensure high-quality deliverables. The Senior Principal Statistical Programmer will be responsible for all statistical programming aspects of several studies, a medium to large sized project or project-level activities. Acts as a key collaborator and strategic partner in ensuring that drug-development plans are executed efficiently with timely and high-quality deliverables. Complies with … project/study standards and specifications following internal and regulatory guidelines. Oversees programming style, quality of statistical reporting & compliance with timelines. About the Role Key requirements Lead statistical programming activities for a medium to large sized project in phase I to IV clinical studies in Novartis Global Development Organization. Co-ordinate activities of programmers either internally or externally. More ❯

skills, experience and knowledge to advance medicine. We achieve this through flexible, innovative, high-quality solutions for our clients, delivered with integrity. The Role We are looking for a Senior Statistical Programmer to join our Biometrics Department where you will provide programming and statistical support to allocated studies and will be responsible for ensuring that the … rights, safety and well-being are protected and is completed within the agreed project timelines. Key Accountabilities Produces and QCs datasets, tables, figures and listings using SAS, including routine statistical analysis. Liaises with Data Management and statistician to ensure the data needed for statistical output from CRF data is available. Manages the flow of work for allocated studies … all study-related activities are adhered to and flags potential changes in scope, database and programming issues to internal and external study teams and suggests resolutions. Acts as the Statistical Programming point of contact for allocated studies and supports at Sponsor meetings. Attends study team meetings throughout the life of the study to communicate issues that may affect the More ❯

skills, experience and knowledge to advance medicine. We achieve this through flexible, innovative, high-quality solutions for our clients, delivered with integrity. The Role We are looking for a Senior Statistical Programmer to join our Biometrics Department where you will provide programming and statistical support to allocated studies and will be responsible for ensuring that the … rights, safety and well-being are protected and is completed within the agreed project timelines. Key Accountabilities Produces and QCs datasets, tables, figures and listings using SAS, including routine statistical analysis. Liaises with Data Management and statistician to ensure the data needed for statistical output from CRF data is available. Manages the flow of work for allocated studies … all study-related activities are adhered to and flags potential changes in scope, database and programming issues to internal and external study teams and suggests resolutions. Acts as the Statistical Programming point of contact for allocated studies and supports at Sponsor meetings. Attends study team meetings throughout the life of the study to communicate issues that may affect the More ❯

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. This is an exciting time to be a 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 More ❯

Responsible for all statistical programming/data review reporting and analytics development aspects of several studies, a medium to large sized project or project-level activities. Acts as a key collaborator and strategic partner in ensuring that drug-development plans are executed efficiently with timely and high quality deliverables. Complies with project/study standards and specifications following internal … and regulatory guidelines. Oversees programming style, quality of statistical reporting & compliance with timelines. About the Role Our Development Team is guided by our purpose: to reimagine medicine to improve and extend people’s lives. To do this, we are optimizing and strengthening our processes and ways of working. We are investing in new technologies and building specific therapeutic area … us and help give people with disease and their families a brighter future to look forward to. Apply today and welcome to where we thrive together! The Role The Senior Principal Programmer is responsible for all statistical programming aspects of several studies, a medium to large sized project or project-level activities (incl. submission and post-marketing More ❯

Senior Statistical Programmer - UK (Remote/Office/Hybrid) Senior Statistical Programmer - UK (Remote/Office/Hybrid) Get AI-powered advice on this job and more exclusive features. Direct message the job poster from Veramed Principal Talent Acquisition Consultant at Veramed Veramed prides itself on two key areas: providing the highest quality statistics … and programming consultancy for its clients, and giving its employees an industry leading working environment with support and training for career growth. We have an exciting opportunity for Senior Statistical Programmers to join us on a permanent basis in the UK. We can offer home and/or office working, training and support and a competitive package. The … TFLs (in SAS) following specifications, applying good programming practice • Complete and review CDISC Validation tool reports • Ensure the appropriate standards are being applied and adhered to • Familiarisation with simple statistical techniques (e.g. t-test, ANOVA, regression, standard survival) • Review of project management related documents • Maintain study master file documents and any other documents that are required to be audit More ❯

Social network you want to login/join with: We’re CRO Solutions, a fast-growing UK-based CRO redefining how statistical programming is done. We're on a mission to improve the way clinical data is handled, analysed, and delivered, and we’re looking for a Senior Statistical Programmer who wants to shape the future … us reimagine processes, develop macros, and improve efficiency. What We Are Looking For : You don’t need to tick every box, but here’s our ideal candidate: Solid SAS programmer with experience leading clinical trial work (minimum of 2 years leading). Confident with CDISC SDTM and ADaM implementation. Comfortable working across departments and leading timelines/resources. Background … learn what you want in your next role. 5 Minute Self-assessment - rate your experience but don’t worry, there are no trick questions. Formal interview with Head of Statistical Programming, our Head of Ops, and Head of Biometrics. 1-hour practical task - test your real skills, not your memory. What CRO Solutions Will Offer You: Annual bonus. More ❯

you’ll also be helping to save the planet! THE ROLE Demand for our Functional Service Provision is growing, therefore we are looking for an experienced, ambitious and driven Programmer to join our Center of Excellence and submissions team. The expectation is that the candidate has very strong CDISC knowledge. As Senior/Principal Programmer, you will … direct experience of working within a pharmaceutical environment. Responsibilities Employees may be required to perform some or all of the following: Program complex non efficacy outputs/figures Perform Senior Review and Deliver QC of non- statistical output Develop and debug complex macros Become involved in developing the standard macro library and take responsibility to implement standard macros … Lead a team for furthering programming development Ensure the principles in the PHASTAR checklist are followed rigorously Archive study documentation following instructions in supplied SOPs Act as a Lead programmer on multiple studies under same project, ensuring quality and timely delivery Liaise with Study Statistician and Project Manager regarding resourcing and deliverables Responsible for study level resources Attend and More ❯

Social and Governance (ESG) initiatives. So, not only would you get your dream job, you'll also be helping to save the planet! THE ROLE We are seeking a Senior Programmer to work across multiple clinical and non-clinical studies; supporting regulatory submission activities; producing and validating datasets and outputs to excellent quality whilst adhering to deliverable timelines. … Excellent knowledge of CDISC SDTM and ADaM implementation guidelines working independently in this area; producing, reviewing and updating complex dataset specifications (including efficacy); creating and debugging complex macros; reviewing Statistical Analysis Plans (SAPs), including study specific ISS/ISE and DSMB SAPs and output shells with a view to commenting from a programming perspective. Excellent team work ethos, proactive … to events throughout the year. Responsibilities Program and validate datasets and SDTMs, including complex efficacy, labs, etc. Become independent technical expert Program complex non efficacy outputs/figures Perform Senior Review and Deliver QC of non- statistical output Become involved in developing the standard macro library and take responsibility to implement standard macros within a study Validate and More ❯

IQVIA is looking to appoint statistical programmers to utilize the SAS programming language to develop clinical study report materials according to the objectives of a clinical trial for regulatory submissions. Programming and performing related tasks serving the full spectrum of statistical programming needs in our DS3 environment (home based): Responsibilities: Import data from various sources Program quality control … data and reporting data issues Interpret project level requirements and develop programming specifications Write programming code following established Good Programming Practices Program SDTM and ADaM datasets Program to create statistical analysis tables, listing and figures Validate datasets and all statistical outputs per prescribed gate checks Communicate with internal and client statisticians and clinical team members to ensure appropriate … standards, SOPs, and standard methodologies Export data and clinical study report materials Provide training and mentoring to team members and department staff You can help us bring clinical trial statistical analysis into the next generation. Award winning and innovative, we will give you access to cutting-edge in-house technology, allowing you to work on global projects across therapeutic More ❯

JOB RESPONSIBILITIES: Support and/or lead programmer for programming and QC of analysis datasets, TFLs or standard tools following Regeneron standard data models or user requirements. Assist in the coordination of activities and communicate shifting timelines and milestones. Integration of data across studies in support of CSS/CSE. Create, manage and maintain the programming specifications for the … and annual reports. If applicable, develop and provide department training for applications and standard tools developed by the department functions group. Provide programming support for simple presentations and basic statistical ad-hoc requests. Assist in the more complex data presentations. Participate in department working groups; provide input in development of tools and improvement of processes. JOB REQUIREMENTS: Education Masters More ❯

Social network you want to login/join with: Senior Statistical Programmer - UK (Remote/Office/Hybrid), Ashton-under-Lyne Client: Veramed Location: Ashton-under-Lyne, United Kingdom Job Category: Other - EU work permit required: Yes Job Views: 4 Posted: 26.04.2025 Expiry Date: 10.06.2025 Job Description: Veramed prides itself on providing high-quality statistics and programming … consultancy, along with an industry-leading working environment supporting career growth. We are seeking a Senior Statistical Programmer for a permanent position in the UK, offering flexible working arrangements, training, support, and a competitive package. The role involves providing programming support across various projects, clients, and therapeutic areas. Key Responsibilities Technical Perform consistency reviews of clinical trial … checks and exploration (e.g., frequencies, histograms) Program and QC datasets and TFLs in SAS following specifications and good practices Review CDISC Validation reports Ensure standards compliance Familiar with basic statistical techniques (e.g., t-test, ANOVA, regression, survival analysis) Review project management documents Maintain audit-ready study documents General Lead and present at study team meetings Share knowledge within the More ❯

Social network you want to login/join with: Senior Statistical Programmer - UK (Remote/Office/Hybrid), London (City of London) col-narrow-left Client: Veramed Location: London (City of London), United Kingdom Job Category: Other - EU work permit required: Yes col-narrow-right Job Views: 4 Posted: 05.05.2025 Expiry Date: 19.06.2025 col-wide Job Description … Veramed prides itself on providing high-quality statistics and programming consultancy, along with an industry-leading working environment supporting career growth. We have an exciting opportunity for a Senior Statistical Programmer to join us on a permanent basis in the UK. We offer flexible working options, training, support, and a competitive package. The role involves providing programming … data checks and exploration (e.g., frequencies, histograms) Program and QC datasets and TFLs in SAS following specifications Review CDISC Validation reports Ensure standards are adhered to Familiarise with basic statistical techniques (e.g., t-test, ANOVA, regression, survival analysis) Review project management documents Maintain study master files and audit-ready documents General Lead study team meetings effectively Present study updates More ❯

Social network you want to login/join with: Senior Statistical Programmer - UK (Remote/Office/Hybrid), United Kingdom Client: Veramed Location: United Kingdom Job Category: Other EU work permit required: Yes Job Views: 4 Posted: 26.04.2025 Expiry Date: 10.06.2025 Job Description: Veramed prides itself on providing high-quality statistics and programming consultancy, along with an … industry-leading working environment that supports career growth. We are offering a permanent position for a Senior Statistical Programmer in the UK, with options for home, office, or hybrid work, along with training, support, and a competitive package. The role involves providing programming support across various projects, clients, and therapeutic areas within the statistics and programming department. … e.g., frequencies, histograms) Program and QC datasets and TFLs in SAS following specifications and good programming practices Complete and review CDISC Validation reports Ensure standards compliance Familiarity with basic statistical techniques (e.g., t-test, ANOVA, regression, survival analysis) Review project management documents Maintain study master files and audit-ready documents General Lead and facilitate internal and client study meetings More ❯

Social network you want to login/join with: Senior Statistical Programmer - UK (Remote/Office/Hybrid), Preston, Lancashire Client: Veramed Location: Preston, Lancashire, United Kingdom Job Category: Other EU work permit required: Yes Job Views: 4 Posted: 06.06.2025 Expiry Date: 21.07.2025 Job Description: Veramed prides itself on providing high-quality statistics and programming consultancy, along … with an industry-leading working environment supporting career growth. We are seeking Senior Statistical Programmers for a permanent role in the UK. We offer flexible working arrangements, training, support, and a competitive package. The role involves providing programming support to the statistics and programming department across various projects, clients, and therapeutic areas. Key Responsibilities Technical Review clinical trial … checks and exploration using tools like frequencies and histograms Program and QC datasets and TFLs in SAS following specifications Review CDISC Validation reports Ensure standards compliance Familiarity with basic statistical techniques Review project management documents Maintain audit-ready study master files General Lead study team meetings and present updates Share knowledge within the team Ensure compliance with applicable regulations More ❯

Social network you want to login/join with: Senior Statistical Programmer - UK (Remote/Office/Hybrid), Cambridge Client: Veramed Location: UK Job Category: Other EU work permit required: Yes Job Views: 4 Posted: 06.06.2025 Expiry Date: 21.07.2025 Job Description: Veramed prides itself on providing high-quality statistics and programming consultancy, along with an industry-leading … working environment supporting career growth. We are seeking Senior Statistical Programmers in the UK for a permanent position. We offer flexible working arrangements, training, support, and a competitive package. The role involves providing programming support across various projects, clients, and therapeutic areas. Key Responsibilities Technical Perform consistency review of clinical trial documents (protocols, SAPs, CRFs, CSRs) Author and … standards Conduct data checks and exploration (e.g., frequencies, histograms) Program and QC datasets and TFLs in SAS following specifications Review CDISC Validation reports Ensure standards compliance Familiarity with basic statistical techniques (t-test, ANOVA, regression, survival analysis) Review project management documents Maintain audit-ready study documents General Lead study team meetings Present study updates Share knowledge within the team More ❯

Social network you want to login/join with: Senior Statistical Programmer - UK (Remote/Office/Hybrid), Milton Keynes Client: Veramed Location: Job Category: Other - EU work permit required: Yes Job Views: 4 Posted: 06.06.2025 Expiry Date: 21.07.2025 Job Description: Veramed prides itself on providing high-quality statistics and programming consultancy, along with an industry-leading … work environment supporting career growth. We have an exciting opportunity for Senior Statistical Programmers in the UK. We offer home, office, or hybrid working, training, support, and a competitive package. The role involves providing programming support across various projects, clients, and therapeutic areas. Key Responsibilities Technical Perform consistency review of clinical trial documents including protocols, SAPs, CRFs, CSRs … dataset standards Perform data checks and exploration using SAS Program and QC datasets and TFLs following specifications Complete and review CDISC validation reports Ensure standards compliance Familiar with basic statistical techniques (e.g., t-test, ANOVA, regression, survival analysis) Review project management documents Maintain audit-ready study documents General Lead study team meetings and present updates Share knowledge within the More ❯

Social network you want to login/join with: Senior Statistical Programmer - UK (Remote/Office/Hybrid), York Client: Veramed Location: Job Category: Other - EU work permit required: Yes Job Views: 4 Posted: 06.06.2025 Expiry Date: 21.07.2025 Job Description: Veramed prides itself on providing high-quality statistics and programming consultancy, along with an industry-leading working … environment supporting career growth. We are seeking Senior Statistical Programmers for a permanent role in the UK, offering home and/or office working, training, support, and a competitive package. The role involves providing programming support to the statistics and programming department across various projects, clients, and therapeutic areas. Key Responsibilities Technical Perform consistency review of clinical trial … tools like frequencies and histograms Program and QC datasets and TFLs in SAS following specifications Complete and review CDISC Validation reports Ensure standards are adhered to Familiar with basic statistical techniques (t-test, ANOVA, regression, survival analysis) Review project management documents Maintain audit-ready study master files General Lead and participate in study team meetings Present updates to internal More ❯

Social network you want to login/join with: Senior Statistical Programmer - UK (Remote/Office/Hybrid), Chelmsford Client: Veramed Location: Job Category: Other - EU work permit required: Yes Job Views: 4 Posted: 06.06.2025 Expiry Date: 21.07.2025 Job Description: Veramed prides itself on providing high-quality statistics and programming consultancy, along with an industry-leading working … environment supporting career growth. We are seeking Senior Statistical Programmers for a permanent role in the UK. We offer flexible working arrangements, training, support, and a competitive package. The role involves providing programming support to the statistics and programming department across various projects, clients, and therapeutic areas. Key Responsibilities Technical Perform consistency reviews of clinical trial documents including … and exploration (e.g., frequencies, histograms) Program and QC datasets and TFLs in SAS following specifications Complete and review CDISC Validation reports Ensure standards are adhered to Familiarity with basic statistical techniques (e.g., t-test, ANOVA, regression, survival analysis) Review project management documents Maintain audit-ready study master files and related documents General Lead study team meetings Present study updates More ❯

Social network you want to login/join with: Senior Statistical Programmer - UK (Remote/Office/Hybrid), Norwich Client: Veramed Location: Job Category: Other - EU work permit required: Yes Job Views: 4 Posted: 06.06.2025 Expiry Date: 21.07.2025 Job Description: Veramed prides itself on providing high-quality statistics and programming consultancy, along with an industry-leading working … environment that supports career growth. We have an exciting opportunity for Senior Statistical Programmers to join us on a permanent basis in the UK. We offer home and/or office working, training, support, and a competitive package. The role involves providing programming support across various projects, clients, and therapeutic areas. Key Responsibilities Technical Perform consistency review of … data checks and exploration (e.g., frequencies, histograms) Program and QC datasets and TFLs in SAS following specifications Complete and review CDISC Validation reports Ensure standards compliance Familiarise with basic statistical techniques (e.g., t-test, ANOVA, regression, survival analysis) Review project management documents Maintain audit-ready study master files and related documents General Lead internal and client study meetings Present More ❯

Social network you want to login/join with: Senior Statistical Programmer - UK (Remote/Office/Hybrid), Plymouth Client: Veramed Location: Plymouth, United Kingdom Job Category: Other EU work permit required: Yes Job Views: 4 Posted: 06.06.2025 Expiry Date: 21.07.2025 Job Description: Veramed prides itself on providing high-quality statistics and programming consultancy, along with an … industry-leading working environment supporting career growth. We have an exciting opportunity for Senior Statistical Programmers to join us on a permanent basis in the UK. We offer home and/or office working, training, support, and a competitive package. The role involves providing programming support to the statistics and programming department across various projects, clients, and therapeutic … exploration (e.g., using frequencies, histograms) Program and QC datasets and TFLs in SAS following specifications Complete and review CDISC Validation reports Ensure standards are adhered to Familiar with simple statistical techniques (e.g., t-test, ANOVA, regression, survival analysis) Review project management documents Maintain audit-ready study master files and related documents General Lead internal and client study meetings effectively More ❯