1 to 25 of 27 Senior Statistical Programmer Jobs in London

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 ❯

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 ❯

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 ❯

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), 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: 04.06.2025 Expiry Date: 19.07.2025 col-wide Job Description … 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. … 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: Senior Statistical Programmer - UK (Remote/Office/Hybrid), south west london col-narrow-left Client: Veramed Location: south west london, United Kingdom Job Category: Other - EU work permit required: Yes col-narrow-right Job Views: 3 Posted: 06.06.2025 Expiry Date: 21.07.2025 col-wide Job Description: Veramed prides … 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. … 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 ❯

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 a Senior Statistical Programmer to join us on a permanent basis in the UK. We can offer home and/or office working, training and support and a competitive … 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: Senior Statistical Programmer, south west london col-narrow-left Client: Warman O'Brien Location: south west london, United Kingdom Job Category: Other - EU work permit required: Yes col-narrow-right Job Views: 15 Posted: 06.06.2025 Expiry Date: 21.07.2025 col-wide Job Description: Senior/Principal Statistical Programmers | Global CRO | UK | France | Poland | Spain | We are partnering with a market-leading global CRO to recruit a Senior and/or Principal Statistical Programmer for a dynamic and high-impact role. This is not a traditional programming position, we’re looking for an experienced professional with robust, end-to-end programming expertise across multiple … UK, France, Spain, or Poland. What to do next: If this opportunity is of interest, please apply now with your CV as the organisation are looking to welcome the Senior & Principal Statistical Programmers onboard as soon as possible. Not what you’re looking for? Please contact Jo Fornaciari on +44 7488 822 859 for a confidential discussion about More ❯

days ago Be among the first 25 applicants Get AI-powered advice on this job and more exclusive features. Senior/Principal Statistical Programmers | Global CRO | UK | France | Poland | Spain | We are partnering with a market-leading global CRO to recruit a Senior and/or Principal Statistical Programmer for a dynamic and high-impact … the UK, France, Spain, or Poland. What to do next: If this opportunity is of interest, please apply now with your CV as the organisation is looking to onboard Senior & Principal Statistical Programmers as soon as possible. Not what you’re looking for? Please contact Jo Fornaciari on +44 7488 822 859 for a confidential discussion about potential More ❯

Job Opening: Senior Statistical Programmer Hobson Prior is seeking a Senior Statistical Programmer to join our client's team in a remote role based in London, UK . This position involves creating and managing data sets for clinical trials, ensuring accurate data analysis, and developing programming codes to support statistical processes. Responsibilities: Design … and specify data sets for clinical trials. Create and validate data models and statistical reports. Develop and test programming codes for data checks and reports. Provide technical guidance to junior programmers. Improve programming processes and establish standards within therapeutic areas. Key Skills and Requirements: Advanced degree in Statistics or a related field. Proficiency in SAS programming. Familiarity with clinical More ❯

Senior or Principal Statistical Programmer - Submissions Proclinical is seeking a Statistical Programmer - Submissions for a Senior position. This role involves supporting regulatory submissions, producing and validating datasets, and ensuring high-quality outputs within set timelines. The position offers flexibility in work location and requires occasional travel for events. Responsibilities: Program datasets including complex efficacy … and lab data. Serve as an independent technical expert and program complex non-efficacy outputs. Conduct senior reviews and quality control of non-statistical outputs. Develop and implement standard macros and perform user acceptance testing. Create, QC, and update complex dataset specifications for various studies. Provide consultancy and training on SDTM, ADaM, and CRT standards. Stay informed on … on finding exceptional people and matching them with the finest positions across the globe. Proclinical is acting as an Employment Agency in relation to this vacancy. Seniority level Mid-Senior level Employment type Full-time Job function Science Professional Services #J-18808-Ljbffr More ❯

culture, and the driving force behind our success. ICON people have a mission to succeed and a passion that ensures what we do, we do well. As a Principal Statistical Programmer, you will be dedicated to one of our global pharmaceutical clients. Responsibilities Responsibilities You will be responsible for completion of the following: Create, validate, execute and generate … statistical programs consisting of listings, safety and efficacy outputs (analysis datasets, tables, figures) Create and finalise project or departmental level macros Create and finalise programming specifications/mock-ups Generating accurate, complete and consistent outputs in accordance with documented procedures and project specific timelines Leading programming deliverables for at least one study of moderate complexity and/or scope … planning Tracking and work allocation to ensure project, timeline and quality goals are consistently achieved. Additionally, you will contribute to the review and quality control of programming deliverables, including statistical programs and supporting specifications and documentation. You will effectively liaise with other functions in the conduct of programming activities and support other project activities such as addressing audit findings More ❯

Senior Statistical Programmer, united kingdom Client: Warman O'Brien Location: Job Category: Other EU work permit required: Yes Job Views: 6 Posted: 06.04.2025 Expiry Date: 21.05.2025 Job Description: Senior Statistical Programmer – FSP | Global CRO | Fully Remote | UK | Europe | A globally recognized CRO is seeking an experienced Senior Statistical Programmer to join … track progress to meet project timelines and quality standards. Key Responsibilities: Lead programming for multiple complex studies. Develop datasets, tables, figures, and listings. Requirements: 5+ years of experience in statistical programming. Proficiency in SAS; knowledge of R is a bonus. Familiarity with CDISC standards (SDTM, ADaM). Strong communication and teamwork skills. Focus on personal development and training. Apply More ❯

days ago Be among the first 25 applicants Get AI-powered advice on this job and more exclusive features. Senior Statistical Programmer I - Join a World-Leading CRO! Join a globally renowned CRO that is expanding its Statistical Programming team across the UK and Europe. This innovative organisation is driven by excellence and firmly believes in … investing in its people, recognizing them as its greatest strength and the driving force behind its success. As a Senior Statistical Programmer I, you will lead studies of varying complexity, working alongside some of the brightest experts in the industry. You will play a significant part of the planned technology expansion journey, gaining exposure to other languages … such as R or Python. What you’ll be doing: Lead Phase II/III studies, crafting, validating, and executing statistical programs for listings, safety, efficacy outputs, and ADaM/TLF specifications. Oversee multi-disciplinary teams, ensuring seamless execution of assigned projects. Design, develop, validate, and execute high-quality SAS programming outputs, including listings, tables, figures, and analysis datasets. More ❯

who collaborate together as one, 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 the 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 knowledge in SAS and CDISC across all phases and multiple therapy areas. What you will … you will bring to the role The job holder must be computer literate and numerate with a willingness to adapt to various computer systems. Hands-on expert level project statistical programmer experienced in providing programming leadership to projects. Statistical programming skills and knowledge across a broad range of applications together with key competencies in customer focus, delivering More ❯

Social network you want to login/join with: Senior Statistical Programmer I, west london col-narrow-left Client: Warman O'Brien Location: west london, United Kingdom Job Category: Other - EU work permit required: Yes col-narrow-right Job Views: 2 Posted: 31.05.2025 Expiry Date: 15.07.2025 col-wide Job Description: Senior Statistical Programmer I … Join a World-Leading CRO! Join a globally renowned CRO that is expanding its Statistical Programming team across the UK and Europe. This innovative organisation is driven by excellence and firmly believes in investing in its people, recognizing them as its greatest strength and the driving force behind its success. As a Senior Statistical Programmer I … planned technology expansion journey, gaining exposure to other languages such as R or Python. What you’ll be doing: Lead Phase II/III studies, crafting, validating, and executing statistical programs for listings, safety, efficacy outputs, and ADaM/TLF specifications. Oversee multi-disciplinary teams, ensuring seamless execution of assigned projects. Design, develop, validate, and execute high-quality SAS More ❯