Jobs at Cytel

As a Senior Statistical Programmer, you will leverage SAS programming skills and CDISC standards to support clinical trials, perform data manipulation, and generate reports.

The Principal Statistical Programmer will independently manage statistical programming for clinical trials, overseeing CRO deliverables, generating datasets, and ensuring compliance with FDA regulations.

The Principal Statistical Programmer will generate datasets and reports, oversee CRO's programming deliverables, and ensure compliance with FDA regulations, while collaborating with various teams in clinical trials.

This role involves managing project operations, supporting leaders with scope reconciliations and invoicing, ensuring documentation compliance, and facilitating team collaboration.

The Principal Statistical Programmer develops and validates SAS and R programs, oversees CRO deliverables, and ensures high-quality statistical reporting for clinical trials.

The Clinical Data Engineer serves as an expert in USDM, driving digital protocol generation and enabling seamless data flow across the clinical development lifecycle, while collaborating across functions to optimize processes and ensure compliance with industry standards.

The Senior Clinical Data Manager oversees data management tasks from study initiation to database lock, ensuring high-quality data delivery, adherence to timelines and budgets, and leading project activities with minimal supervision. Responsibilities include user acceptance testing, data cleaning, project documentation, training staff, and managing client communication.

The Senior Statistical Programmer will support and lead clinical trials by performing data manipulation, analysis, and reporting using SAS programming. Responsibilities include generating SDTM and ADaM datasets, validating programming, creating reports, and collaborating with cross-functional teams.

The Principal Statistical Programmer provides technical leadership in SAS and R programming for clinical trial data analysis, reporting, and regulatory submissions, ensuring compliance and quality control while managing teams and resources.

The Principal Statistical Programmer leads SAS and R programming for clinical trials, ensuring compliance, quality, and effective communication with stakeholders.

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.

The Principal Statistical Programmer oversees clinical trial programming, implementing reporting and analysis for pharmaceutical clients while ensuring quality and regulatory compliance.

As a Senior Statistical Programmer, you will perform data manipulation and analysis for clinical trials, generate SDTM and ADaM datasets, ensure quality control, and communicate with project teams while potentially leading multiple projects.

The Senior Statistical Programmer will use advanced SAS skills to support Phase I-IV clinical trials, generate datasets, and lead data analyses.

The Senior Statistical Programmer will conduct data manipulation, analysis, and reporting for clinical trials using SAS. This role involves generating SDTM/ADaM datasets, performing QC, and leading project tasks while collaborating with cross-functional teams.

The Senior Statistical Programmer will manage clinical trial data using advanced SAS skills, ensuring quality through data analysis, manipulation, and reporting, while adhering to CDISC standards and collaborating with cross-functional teams.

Lead statistical activities for clinical trials, collaborate with stakeholders, oversee programming and junior statisticians, and apply statistical methods for data analysis.

The Principal Statistical Programmer oversees programming activities for clinical trials, ensuring high-quality data summaries and compliance with statistical standards while mentoring CRO programmers.

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.