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14 of 14 Principal Statistical Programmer Jobs in London
London, England, United Kingdom Hybrid / WFH Options AL Solutions
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 … 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 multiple studies or an entire program. Develop and validate SAS programs for the creation of SDTM, ADaM datasets, and TLFs (tables, listings, figures). Ensure compliance with CDISC standards and regulatory requirements. Mentor and support junior programmers and More ❯
London, England, United Kingdom Hybrid / WFH Options Warman O'Brien
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 … 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 … 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 More ❯
Hounslow, England, United Kingdom Hybrid / WFH Options JR United Kingdom
Social network you want to login/join with: Principal 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: 5 Posted: 06.06.2025 Expiry Date: 21.07.2025 … col-wide Job Description: Principal Statistical Programmer | Leading CRO | UK | Home Based | Permanent | Award winning global CRO have a new opportunity for a Principal Statistical Programmer to join their dynamic and expanding team. This is a fully home-based position based in the UK. … This is a Statistical Programming leadership role with responsibility for one high complexity programming project or at least two moderate complexity studies. You will be involved in effective resource planning, work allocation and progress tracking to ensure project timelines and quality targets are consistently achieved. In this client-facing More ❯
London, England, United Kingdom Hybrid / WFH Options Novartis
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 … 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. More ❯
London, England, United Kingdom TREIZE-QUARANTE (1340)
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 … 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 More ❯
London, England, United Kingdom Novartis Farmacéutica
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 … 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 More ❯
London, England, United Kingdom Novartis
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 … 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 More ❯
London, England, United Kingdom Hybrid / WFH Options Novartis
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 … 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 … 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 More ❯
Kensington, England, United Kingdom TFS HealthScience
companies throughout their clinical development journey. Our expertise includes full service capabilities, resourcing, and Functional Service Provider (FSP) solutions. Join Our Team as a Principal Statistical Programmer About this role As part of our Global Biometrics Department , you will work alongside passionate and innovative professionals to help … our customers achieve their goals. The Principal Statistical Programmer is responsible for preparing, conducting, and completing programming tasks (mainly in SAS) in assigned Study Teams according to company policies, SOPs, and regulatory requirements. Key Responsibilities: Mentoring Statistical Programmers and Senior Statistical Programmers Acting as a … within assigned studies or leading programming efforts for a study or program Producing programming outputs such as: Edit checks Listings Summary tables Graphics Performing statistical tests (if background in Statistics) Other duties as assigned Qualifications: Bachelor’s Degree in computer science, statistics, or equivalent Minimum 8 years of relevant More ❯
London, England, United Kingdom Hybrid / WFH Options TFS HealthScience
companies throughout their clinical development journey. Our expertise includes full-service capabilities, resourcing, and Functional Service Provider (FSP) solutions. Join Our Team as a Principal Statistical Programmer About this role As part of our Global Biometrics Department , you will work alongside passionate and innovative professionals to help … our clients achieve their goals. The Principal Statistical Programmer is responsible for preparing, conducting, and completing programming tasks (mainly in SAS) within assigned Study Teams, following company policies, SOPs, and regulatory requirements. Key Responsibilities: Mentoring Statistical Programmers and Senior Statistical Programmers Potentially acting as a … within studies or leading programming efforts for a study/program Producing programming outputs such as edit checks, listings, summary tables, and graphics Conducting statistical tests (if background in Statistics) Qualifications: Bachelor's Degree, preferably in computer science, statistics, or equivalent Minimum 8 years of relevant programming experience (preferably More ❯
City of London, England, United Kingdom Proclinical Staffing
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 … 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 More ❯
London, England, United Kingdom Hybrid / WFH Options Novartis
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 … 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 More ❯
London, England, United Kingdom Hybrid / WFH Options Novartis Farmacéutica
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 … 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. More ❯
London, England, United Kingdom PHASTAR
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 … 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 ❯
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