London, England, United Kingdom Hybrid / WFH Options
ZipRecruiter
clients, and giving its employees an industry leading working environment with support and training for career growth. We have an exciting opportunity for a SeniorStatisticalProgrammer to join us on a permanent basis in the UK. We can offer home and/or office working, training … 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 ❯
London, England, United Kingdom Hybrid / WFH Options
IQVIA
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 ❯
So, not only would you get your dream job, you'll also be helping to save the planet! THE ROLE We are seeking a SeniorProgrammer to work across multiple clinical and non-clinical studies; supporting regulatory submission activities; producing and validating datasets and outputs to excellent quality … 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. … 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 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 … 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 More ❯
Ashton-under-Lyne, England, United Kingdom Hybrid / WFH Options
ZipRecruiter
its clients, and giving its employees an industry leading working environment with support and training for career growth. We have an exciting opportunity for SeniorStatistical Programmers to join us on a permanent basis in the UK. We can offer home and/or office working, training 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 ❯
Aberdeen, Scotland, United Kingdom Hybrid / WFH Options
JR United Kingdom
its clients, and giving its employees an industry leading working environment with support and training for career growth. We have an exciting opportunity for SeniorStatistical Programmers to join us on a permanent basis in the UK. We can offer home and/or office working, training 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 ❯
Leicester, England, United Kingdom Hybrid / WFH Options
JR United Kingdom
its clients, and giving its employees an industry leading working environment with support and training for career growth. We have an exciting opportunity for SeniorStatistical Programmers to join us on a permanent basis in the UK. We can offer home and/or office working, training 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 ❯
Cheltenham, England, United Kingdom Hybrid / WFH Options
JR United Kingdom
its clients, and giving its employees an industry leading working environment with support and training for career growth. We have an exciting opportunity for SeniorStatistical Programmers to join us on a permanent basis in the UK. We can offer home and/or office working, training 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 ❯
Derby, England, United Kingdom Hybrid / WFH Options
JR United Kingdom
its clients, and giving its employees an industry leading working environment with support and training for career growth. We have an exciting opportunity for SeniorStatistical Programmers to join us on a permanent basis in the UK. We can offer home and/or office working, training 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 ❯
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 … 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 More ❯