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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 structures, and ensure 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’ needs … 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, on-time … 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 or externally. More ❯

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 Phase I … 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 ❯

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. Make statistical 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 be … 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 within a study Create, QC and update complex … 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 ❯

Senior 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 several 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, on-time deliverables. This includes developing and validating SDTM and ADaM … while ensuring proper documentation and compliance with SOPs. What you will need: A Master’s or Ph.D. degree in Statistics, Biostatistics or Computer Sciences and 6 years’ experience in statistical programming. OR A Bachelor’s degree in the above fields with at least 6 years’ experience in clinical trial statistical programming. Excellent knowledge of SAS essential with R More ❯

week ago Be among the first 25 applicants Get AI-powered advice on this job and more exclusive features. 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 … 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 ❯

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 purpose of 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 ❯

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 clinical trial … 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 ❯

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 clinical trial … 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 ❯

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 … 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 activities). The More ❯

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 be performed as More ❯

Join to apply for the Principal Statistical Programmer FSP role at TREIZE-QUARANTE (1340) . Get AI-powered advice on this job and more exclusive features. Position Overview The Principal Statistical Programmer works independently with minimal supervision, tracking progress and providing expert technical support to team members. The role involves working on clinical development programs across … validation. Review and author data transfer specifications for external vendors. Collaborate with internal and external partners to meet project timelines. Review and author SOPs and work instructions related to statistical programming. Qualifications Bachelor's degree in computer science, data science, mathematics, or statistics. 7+ years of experience as a Statistical Programmer in a clinical development environment. Expertise … in SAS programming and clinical statistical procedures. Extensive experience with CDISC standards and regulatory requirements. Experience supporting regulatory submissions and HTA dossiers is a plus. Ability to work independently with excellent communication and leadership skills. Preferred Skills Proficiency in R, Python, Java, Shiny, Markdown, Unix/Linux, git. Additional Details Location: London, England, United Kingdom Employment type: Full-time 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 ❯

Senior Statistical SAS Programmer - home- or office-based, EMEA Pay Competitive Employment type Full-Time Job Description Req#: 2260641 As an experienced Statistical SAS Programmer in our Clinical Development Services (CDS) business unit, you are central to the successful delivery of complex clinical trials for renowned, innovative and global top pharmaceutical and biotech companies. Oftentimes you … new benchmark drugs for a wide variety of therapeutic areas such as oncology, cardiovascular, respiratory, neurological, diabetes, rare diseases, pain, immunology etc. Your expertise and your work as a statistical programmer has a direct impact on improving the health and lives of thousands of patients around the globe every day. Join us and see why more than … support SDTMs and ADaMs Respond to QA and client audits and support qualification audits Identify and propose innovative ways to improve the efficiency, quality and productivity of our clinical statistical programming business Maintain awareness of industry standards, global regulatory requirements, internal guidelines and Standard Operating Procedures (SOPs) Your profile: Degree in a relevant field such as mathematics, life sciences More ❯

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 at managing … 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 perform User Acceptance Testing (UAT) on standard macros 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 ❯

applicants Direct message the job poster from AL Solutions Expert in linking Biometrics, Biologics and CMC Professionals to Biotech and CDMOs throughout the United States and Canada. Position: Principal Statistical Programmer Location: Remote, UK Are you an experienced Statistical Programmer looking to take the next step in your career? Join a leading, award-winning global CRO … that partners with top biopharmaceutical companies to drive innovative clinical research across multiple therapeutic areas. George Higginson and his team are seeking a Principal Statistical Programmer to provide leadership and technical expertise on complex interventional studies and programs. This is a remote-based role open to candidates across the UK. Main Responsibilities: Lead statistical programming activities across … junior programmers and contribute to departmental process improvement initiatives. Act as the primary programming contact for clients and internal project teams. Requirements: Over 8 years of experience as a Statistical Programmer within a CRO, Biotech or Pharma. Bachelor’s or Master’s degree in a scientific, statistical, or related discipline. Extensive experience with SAS programming in a More ❯

We are currently partnered with a Global Mid-sized Pharmaceutical Company who are seeking a Statistical Programmer to join their Programming department. You would be working for a pharmaceutical company offering a full remote role and they have a good retention rate in the industry. They offer an inspiring place to work and a chance to make your … mark in doing good for others with an open and progressive culture experience. They are looking for a candidate with 8+ years of Statistical Programming experience and extensive Oncology experience. Substantial experience in clinical data standards ADAMS, TLFs, and submission guidelines, and hands-on programming experience within one or more statistical/data science programming languages (e.g., R … effectively, including teaching/explaining data-driven results to others. Substantial experience in clinical data standards ADAMS, TLFs, and submission guidelines. Hands-on programming experience within one or more statistical/data science programming languages (e.g., R, SAS, or Python). Knowledge of the data science lifecycle and process flow (e.g., ETL, data quality, statistical data analysis, machine More ❯

Join to apply for the Principal Statistical Programmer role at Novartis . 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, and compliance with timelines. About The Role Our Development Team is guided by our purpose: to reimagine medicine to improve and extend people’s lives. We are optimizing and strengthening our processes and ways … you to join us in giving people with disease and their families a brighter future. Apply today and join a place where we thrive together! The Role The Principal Statistical Programmer is responsible for all statistical programming aspects of large/pivotal studies, several studies, or project-level activities, including submission activities. The role involves collaboration with 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, stockport col-narrow-left Client: Warman O'Brien Location: stockport, 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, peterborough col-narrow-left Client: Warman O'Brien Location: peterborough, 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, northampton col-narrow-left Client: Warman O'Brien Location: northampton, 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 ❯