Jobs at Cytel

As a Senior Statistical Programmer, you'll manipulate and analyze clinical trial data using SAS, generate CDISC-compliant datasets, and support clinical projects, ensuring quality and adherence to standards.

Lead or support Phase I-IV clinical trial programming using SAS and CDISC standards to generate and validate SDTM/ADaM datasets, produce TLFs, perform QC/validation, create submission documents (define.xml), and communicate with cross-functional teams. Provide ad-hoc reports, efficacy analyses, and occasional study lead duties while working collaboratively in a global, remote environment.

The Senior Statistical Programmer will manage and report on clinical trial data, generating SDTM/ADaM datasets and collaborating with cross-functional teams in a pharmaceutical setting.

Lead sponsor-dedicated statistical programming for clinical trials: create SDTM/ADaM specifications and datasets, develop and validate SAS programs, oversee CRO deliverables, support regulatory submissions and study reports, maintain programming standards, and collaborate across clinical and vendor teams.

As a Senior Statistical Programmer, you'll manage clinical trial data analysis and reporting, ensuring adherence to CDISC standards and statistical methodologies.

Lead statistical programming for sponsor clinical trials: develop SDTM/ADaM specs and datasets, author validated SAS/R programs, oversee CRO deliverables, support regulatory submissions, and maintain programming standards and SOPs.

Lead or support Phase I-IV clinical trial programming using advanced SAS and CDISC (SDTM/ADaM). Produce and validate SDTM/ADaM datasets, TLFs, define.xml and submission documents, perform QC/validation, ad-hoc reporting, efficacy analyses, and collaborate with cross-functional teams. Serve as study lead when required and deliver high-quality outputs on tight timelines.

The Principal Statistical Programmer leads statistical programming efforts for clinical trials, ensuring high-quality data analysis using SAS and R. Responsibilities include generating datasets, overseeing deliverables from CROs, and adhering to regulatory standards.

The Principal Statistical Programmer will generate CDISC datasets, develop SAS and R programs, oversee CRO deliverables, and ensure high-quality statistical analysis for clinical trials.

The Principal Biostatistician leads clinical studies, provides statistical expertise for trial processes, and collaborates with sponsor teams on HTA submissions.

As a Senior Statistical Programmer, you will manage clinical trial data analysis, utilizing SAS, generating reports, and adhering to CDISC standards while ensuring quality output within deadlines.