16 of 16 Senior Statistical Programmer Jobs

Parexel is looking for a Senior Statistical (SAS) Programmer to join our FSP team in either the UK, Hungary, Poland or Serbia The Senior Statistical Programmer provides technical expertise for the conduct of clinical trials, acts as an internal subject matter expert in specific … expert advice, and works independently to support various programing activities related to the analysis and reporting of clinical study data. In addition, the Senior Statistical Programmer can fill the Statistical Programming Lead role on projects, and liaise with sponsors, Biostatistics Leads, Data Management Leads, and other ...

patient. We take our work personally, we do it with empathy and we're committed to making a difference.Parexel is looking for a Senior Statistical (SAS) Programmer to join our FSP team in either the UK, Hungary, Poland or SerbiaThe Senior Statistical Programmer provides … expert advice, and works independently to support various programing activities related to the analysis and reporting of clinical study data. In addition, the Senior Statistical Programmer can fill the Statistical Programming Lead role on projects, and liaise with sponsors, Biostatistics Leads, Data Management Leads, and other ...

Senior Clinical Statistical Programmer (Portfolio Development/Biometrics/Programming)The RoleCSL is looking for a Senior Programmer to take technical ownership of one or two clinical trials from first line of code to final submission package. This is a hands-on statistical programming … technical reference point for less experienced programmers, and a contributor to how the wider programming function does its work.· Serve as lead programmer for one or two clinical trials, interpreting protocols, SAPs, data management plans, and CRF specifications to drive study setup and analysis· Design and validate SDTM ...

Senior Clinical Statistical Programmer (Portfolio Development/Biometrics/Programming) The Role CSL is looking for a Senior Programmer to take technical ownership of one or two clinical trials from first line of code to final submission package. This is a hands‐on statistical … technical reference point for less experienced programmers, and a contributor to how the wider programming function does its work. Serve as lead programmer for one or two clinical trials, interpreting protocols, SAPs, data management plans, and CRF specifications to drive study setup and analysis Design and validate SDTM ...

Senior Clinical Statistical Programmer (Portfolio Development/Biometrics/Programming) The Role CSL is looking for a Senior Programmer to take technical ownership of one or two clinical trials from first line of code to final submission package. This is a hands-on statistical … technical reference point for less experienced programmers, and a contributor to how the wider programming function does its work. Serve as lead programmer for one or two clinical trials, interpreting protocols, SAPs, data management plans, and CRF specifications to drive study setup and analysis Design and validate SDTM ...

believe that behind every dataset, every line of code, and every submission package, there's a patient waiting for a better option. As our Senior Statistical Programmer, you are one of the people who makes that happen. This isn't a role where your work disappears into … preparation (think NDA, BLA, MAA) — real regulatory milestones that mark pivotal moments in a medicine's journey Reviewing and shaping key planning documents like Statistical Analysis Plans (SAPs) and Data Presentation Plans, ensuring clarity and completeness before programming work begins - your input genuinely steers project direction Partnering with vendors ...

Senior Clinical Statistical Programmer (Portfolio Development/Biometrics/Programming) The Role CSL is looking for a Senior Programmer to take technical ownership of one or two clinical trials from first line of code to final submission package. This is a hands-on statistical ...

Bristol Myers Squibb in the UK is seeking a Senior Statistical Programmer to drive programming work within our Global Biometrics & Data Sciences function, collaborating with cross-functional clinical teams and external vendors. This role offers autonomy, high-impact projects, and exposure to regulatory submissions; you will produce ...

ClinChoice is seeking a Senior Statistical Programmer Consultant (Oncology) for a remote UK-based position outside IR35. The role involves delivering programming components under leadership, tackling complex clinical programming tasks, and coordinating with study teams to ensure quality and regulatory compliance. The ideal candidate has extensive CDISC ...

ClinChoice is seeking a Principal Statistical Programmer Consultant to join a client-facing team in the United Kingdom. The role emphasizes leading statistical programming activities, delivering SAS programs, and ensuring SDTM/ADaM compliance in regulatory submissions. Ideal candidates have a CS or statistics degree with CDISC ...

Johnson & Johnson in High Wycombe, UK is seeking an Experienced Statistical Programmer to join the Data Analytics & Computational Sciences team. You will develop, verify, and document statistical programs for clinical data, supporting analysis and reporting with high quality deliverables. You will collaborate with cross-functional teams, ensure ...

Worldwide Clinical Trials in the United Kingdom is seeking an experienced Statistical Programmer to lead programming efforts on medium to large-scale studies, ensuring CDISC compliance and high-quality outputs. You will develop and review SDTM/ADaM datasets, TFLs, and deliver analysis-ready data, collaborating with statisticians ...

Worldwide Clinical Trials is seeking a skilled Statistical Programmer to join our Global Programming team. You will develop and validate CDISC SDTM/ADaM datasets, create TFLs and listings, and contribute to submission-ready packages across multiple studies. You will review study specs, lead programming efforts on medium ...

full-service contract research organization providing expertise-based clinical research services to the pharmaceutical, biotechnology, and medical device industries. Everest is seeking a senior SAS Programmer to design data tabulation and analysis data models, develop robust SAS code, validate outputs, and support continuous improvement of statistical programming ...

Parexel is seeking a Senior Statistical (SAS) Programmer to join our FSP team in the UK, Hungary, Poland or Serbia. The role provides technical expertise for clinical trial analysis and reporting, acting as an internal SME and supporting programming activities across study data. You will lead ...

data from multiple trials (e.g. ISS and ISE datasets). These designs and specifications are completed in accordance with common industry standards and conventions, statistical requirements and specifications, and/or clinical trial sponsor’s requirements. Generate complete and efficient analysis data models following approved dataset designs or specifications. … Perform independent validation of datasets created by other programmers or statisticians. Develop SAS programming codes and generate complete and accurate statistical output reports of trial data in well-defined formats. Develop SAS programming codes to independently validate statistical output reports of trial data generated by other programmers ...