26 to 39 of 39 Statistical Programmer Jobs in London

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 … 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 … 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 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 … 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 … 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 More ❯

Job Description Summary 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. Job Description Our Development Team is guided by our purpose: to reimagine medicine to improve and extend people's lives. To do this … disease and their families a brighter future to look forward to. Apply today and welcome to where we thrive together! The Role The Principal Statistical Programmer is responsible for all statistical programming aspects of a large/pivotal study, several studies or project-level activities (including submission 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 … 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 … 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 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 … 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 More ❯

Since 1990, METRONOMIA has stood for quality, competence, continuity and unconditional customer orientation in terms of data management, statistical services and medical writing in clinical research. As a growth-oriented medium-sized company with over 145 employees, we operate internationally. Our customers appreciate the competence and commitment of our … employees and we value our employees as the basis of the company's success. Join a motivated and friendly team as Statistical Programmer (UK Remote) Your responsibilities You program and validate statistical analysis of clinical studies with SAS. You define and program analysis datasets and CDISC SDTM More ❯

Since 1990, METRONOMIA has stood for quality, competence, continuity and unconditional customer orientation in terms of data management, statistical services and medical writing in clinical research. As a growth-oriented medium-sized company with over 145 employees, we operate internationally. Our customers appreciate the competence and commitment of our … employees and we value our employees as the basis of the company's success. Join a motivated and friendly team as Statistical Programmer (UK Remote) Your responsibilities You program and validate statistical analysis of clinical studies with SAS. You define and program analysis datasets and CDISC SDTM 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 role. This is not a traditional programming position; we’re looking for an experienced professional with robust, end-to-end programming expertise across multiple therapeutic areas. The ideal candidate will have a strong background in data anonymization and disclosure, with hands … 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 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 … 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 … 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 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 … 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 … 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 More ❯

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 … 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 More ❯

55m Series B round from Balderton Capital, with support from Creandum, Firstminute, Seedcamp, and Visionaries. About the role Lindus Health are looking for a Statistical Programmer to join our Clinical Biostatistics team. This is a pivotal role in scaling our clinical data capabilities, ensuring efficient and high-quality … can bring a creative and structured approach to transforming raw clinical data into meaningful insights. The ideal candidate will have a deep understanding of statistical programming in R, clinical trial data standards, and regulatory requirements to support high-quality, efficient, and reproducible analyses. You will work closely with our More ❯

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 be fully integrated into our sponsor’s submission excellence team as a key contributor, providing hands-on technical eSUB expertise including guidance, define, reviewer’s guide, for submission of clinical trial data for FDA, PMDA and EMA regulatory agencies. This is a fantastic opportunity to work … 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 within a study More ❯

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 … 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. … 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 perform User Acceptance More ❯