101 to 125 of 266 Statistical Programmer Jobs

Social network you want to login/join with: Principal Statistical Programmer, wolverhampton col-narrow-left Client: Warman O'Brien Location: Job Category: Other - EU work permit required: Yes col-narrow-right Job Views: 4 Posted: 31.05.2025 Expiry Date: 15.07.2025 col-wide Job Description: Principal Statistical Programmer | Leading CRO | Home Based | UK | Join a fast-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 Principal 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, on-time … compliance with SOPs. What you will need: A Bachelor’s degree in Statistics, Biostatistics or Computer Sciences + Masters or PH.D in Statistics. 8 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 ❯

Social network you want to login/join with: Principal Statistical Programmer, basildon col-narrow-left Client: Warman O'Brien Location: basildon, United Kingdom Job Category: Other - EU work permit required: Yes col-narrow-right Job Views: 4 Posted: 31.05.2025 Expiry Date: 15.07.2025 col-wide Job Description: Principal Statistical Programmer | Leading CRO | Home Based | UK | Join … 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 Principal 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, on-time … compliance with SOPs. What you will need: A Bachelor’s degree in Statistics, Biostatistics or Computer Sciences + Masters or PH.D in Statistics. 8 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 ❯

Social network you want to login/join with: Principal Statistical Programmer, norwich col-narrow-left Client: Warman O'Brien Location: Job Category: Other - EU work permit required: Yes col-narrow-right Job Views: 4 Posted: 31.05.2025 Expiry Date: 15.07.2025 col-wide Job Description: Principal Statistical Programmer | Leading CRO | Home Based | UK | Join a fast-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 Principal 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, on-time … compliance with SOPs. What you will need: A Bachelor’s degree in Statistics, Biostatistics or Computer Sciences + Masters or PH.D in Statistics. 8 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 ❯

Social network you want to login/join with: Principal Statistical Programmer, guildford col-narrow-left Client: Warman O'Brien Location: guildford, United Kingdom Job Category: Other - EU work permit required: Yes col-narrow-right Job Views: 4 Posted: 31.05.2025 Expiry Date: 15.07.2025 col-wide Job Description: Principal Statistical Programmer | Leading CRO | Home Based | UK | Join … 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 Principal 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, on-time … compliance with SOPs. What you will need: A Bachelor’s degree in Statistics, Biostatistics or Computer Sciences + Masters or PH.D in Statistics. 8 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 ❯

Social network you want to login/join with: Principal Statistical Programmer, belfast col-narrow-left Client: Warman O'Brien Location: belfast, United Kingdom Job Category: Other - EU work permit required: Yes col-narrow-right Job Views: 4 Posted: 31.05.2025 Expiry Date: 15.07.2025 col-wide Job Description: Principal Statistical Programmer | Leading CRO | Home Based | UK | Join … 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 Principal 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, on-time … compliance with SOPs. What you will need: A Bachelor’s degree in Statistics, Biostatistics or Computer Sciences + Masters or PH.D in Statistics. 8 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 ❯

Social network you want to login/join with: Principal Statistical Programmer, swindon, wiltshire col-narrow-left Client: Warman O'Brien Location: swindon, wiltshire, United Kingdom Job Category: Other - EU work permit required: Yes col-narrow-right Job Views: 4 Posted: 31.05.2025 Expiry Date: 15.07.2025 col-wide Job Description: Principal Statistical Programmer | Leading CRO | Home Based … 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 Principal 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, on-time … compliance with SOPs. What you will need: A Bachelor’s degree in Statistics, Biostatistics or Computer Sciences + Masters or PH.D in Statistics. 8 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 ❯

Social network you want to login/join with: Principal Statistical Programmer, preston, lancashire col-narrow-left Client: Warman O'Brien Location: preston, lancashire, United Kingdom Job Category: Other - EU work permit required: Yes col-narrow-right Job Views: 4 Posted: 31.05.2025 Expiry Date: 15.07.2025 col-wide Job Description: Principal Statistical Programmer | Leading CRO | Home Based … 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 Principal 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, on-time … compliance with SOPs. What you will need: A Bachelor’s degree in Statistics, Biostatistics or Computer Sciences + Masters or PH.D in Statistics. 8 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 ❯

Social network you want to login/join with: Principal Statistical Programmer, oxford district col-narrow-left Client: Warman O'Brien Location: oxford district, United Kingdom Job Category: Other - EU work permit required: Yes col-narrow-right Job Views: 4 Posted: 31.05.2025 Expiry Date: 15.07.2025 col-wide Job Description: Principal Statistical Programmer | Leading CRO | Home Based … 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 Principal 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, on-time … compliance with SOPs. What you will need: A Bachelor’s degree in Statistics, Biostatistics or Computer Sciences + Masters or PH.D in Statistics. 8 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 ❯

Social network you want to login/join with: Principal Statistical Programmer, luton, bedfordshire col-narrow-left Client: Warman O'Brien Location: luton, bedfordshire, United Kingdom Job Category: Other - EU work permit required: Yes col-narrow-right Job Views: 4 Posted: 31.05.2025 Expiry Date: 15.07.2025 col-wide Job Description: Principal Statistical Programmer | Leading CRO | Home Based … 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 Principal 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, on-time … compliance with SOPs. What you will need: A Bachelor’s degree in Statistics, Biostatistics or Computer Sciences + Masters or PH.D in Statistics. 8 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 ❯

Social network you want to login/join with: Principal Statistical Programmer, warrington, cheshire col-narrow-left Client: Warman O'Brien Location: Job Category: Other - EU work permit required: Yes col-narrow-right Job Views: 4 Posted: 31.05.2025 Expiry Date: 15.07.2025 col-wide Job Description: Principal Statistical Programmer | Leading CRO | Home Based | UK | Join a fast … 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 Principal 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, on-time … compliance with SOPs. What you will need: A Bachelor’s degree in Statistics, Biostatistics or Computer Sciences + Masters or PH.D in Statistics. 8 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 ❯

Social network you want to login/join with: Principal Statistical Programmer, sheffield, south yorkshire col-narrow-left Client: Warman O'Brien Location: sheffield, south yorkshire, United Kingdom Job Category: Other - EU work permit required: Yes col-narrow-right Job Views: 4 Posted: 31.05.2025 Expiry Date: 15.07.2025 col-wide Job Description: Principal Statistical Programmer | Leading CRO … 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 Principal 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, on-time … compliance with SOPs. What you will need: A Bachelor’s degree in Statistics, Biostatistics or Computer Sciences + Masters or PH.D in Statistics. 8 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 ❯

Social network you want to login/join with: Principal Statistical Programmer, bolton, greater manchester col-narrow-left Client: Warman O'Brien Location: bolton, greater manchester, United Kingdom Job Category: Other - EU work permit required: Yes col-narrow-right Job Views: 4 Posted: 31.05.2025 Expiry Date: 15.07.2025 col-wide Job Description: Principal Statistical Programmer | Leading CRO … 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 Principal 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, on-time … compliance with SOPs. What you will need: A Bachelor’s degree in Statistics, Biostatistics or Computer Sciences + Masters or PH.D in Statistics. 8 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 ❯

Social network you want to login/join with: Principal Statistical Programmer, stoke-on-trent col-narrow-left Client: Warman O'Brien Location: stoke-on-trent, United Kingdom Job Category: Other - EU work permit required: Yes col-narrow-right Job Views: 4 Posted: 31.05.2025 Expiry Date: 15.07.2025 col-wide Job Description: Principal Statistical Programmer | Leading CRO … 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 Principal 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, on-time … compliance with SOPs. What you will need: A Bachelor’s degree in Statistics, Biostatistics or Computer Sciences + Masters or PH.D in Statistics. 8 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 ❯

Social network you want to login/join with: Principal Statistical Programmer, kingston upon hull, east yorkshire col-narrow-left Client: Warman O'Brien Location: kingston upon hull, east yorkshire, United Kingdom Job Category: Other - EU work permit required: Yes col-narrow-right Job Views: 4 Posted: 31.05.2025 Expiry Date: 15.07.2025 col-wide Job Description: Principal Statistical Programmer | Leading 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’ needs this 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 Principal 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, on-time deliverables. This includes developing and validating SDTM and ADaM datasets, performing 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 support across … 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. Key Responsibilities … 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 ❯

Principal Statistical Programmer | Leading 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’ needs this 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 Principal 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, on-time deliverables. This includes developing and validating SDTM and ADaM … compliance with SOPs. What you will need: A Bachelor’s degree in Statistics, Biostatistics or Computer Sciences + Masters or PH.D in Statistics. 8 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 ❯

Social network you want to login/join with: Principal Statistical Programmer | Leading 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’ needs this 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 Principal 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, on-time … compliance with SOPs. What you will need: A Bachelor’s degree in Statistics, Biostatistics or Computer Sciences + Masters or PH.D in Statistics. 8 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 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, we are optimizing and strengthening our processes and ways of working. We are investing in new technologies and building specific … 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 Principal Statistical Programmer is responsible for all statistical programming aspects of a large/pivotal study, several studies or project-level activities (including submission activities). The position is 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 documents, including … 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 review study … 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 Author and … 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 ❯

Job Title: Senior Statistical Programmer I Career Level - D Introduction to role The Senior Statistical Programmer I is a delivery-focused role responsible for programming deliverables with quality and timeliness, following established standards and processes. This position requires technical skills and adequate industry knowledge to independently perform programming tasks while using judgment about seeking guidance in … will drive continuous improvement. Accountabilities Collaborate with other team members to provide programming support to deliver technical programming and information components of a study or a project deliverable Implement statistical programming aspects of the protocol or clinical development program Ensure high quality is built into own deliverables and the deliverables of other programmers on the team Program independently with … activities and tasks Identify and communicate risk within the assigned studies and/or projects Work cooperatively with study team members including but not limited to the statistician, lead programmer, data manager, and study leader Work cooperatively with contract programming providers Contribute to technical initiatives Employ basic project management practices in managing programming aspects of drug or technical projects More ❯

Social network you want to login/join with: Senior Statistical Programmer - UK (Remote/Office/Hybrid), Greater Manchester Client: Veramed Location: Greater Manchester, UK Job Category: Work abroad, Other EU work permit required: Yes Job Views: 8 Posted: 08.05.2025 Expiry Date: 22.06.2025 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 seeking a Senior Statistical Programmer for a permanent role 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 Perform consistency reviews of clinical trial documents including protocols … tools like frequencies and histograms. Program and QC datasets and TFLs in SAS following specifications and good practices. Review CDISC Validation reports and ensure standards compliance. Familiarity with basic statistical techniques such as t-test, ANOVA, regression, and survival analysis. Review project management documents and maintain audit-ready study files. General Responsibilities Lead and participate in study team meetings 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 documents including … 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 ❯