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The Senior Biostatistician supports clinical studies, develops study protocols, performs statistical analyses, prepares clinical reports, and ensures compliance with FDA regulations.

The Principal Statistical Programmer will generate SDTM/ADaM files, develop SAS programs for clinical trials, oversee CRO deliverables, and ensure compliance with FDA regulations.

The Senior Clinical Data Manager oversees clinical data management from study start-up to database lock, ensuring compliance and quality in deliverables across multiple CROs. Responsibilities include vendor oversight, risk mitigation, regulatory submissions, and managing budgets and timelines for data management activities.

The Vice President of Business Development will lead the global Large Pharma Sales team, drive strategic sales initiatives, and manage client relationships to expand Cytel's client base in the pharmaceutical industry.

As a Principal Statistical Programmer, you will manage statistical programming tasks in clinical trials, ensuring high-quality data reporting and compliance with regulations.

As a Senior Statistical Programmer, you will support or lead clinical trials by performing data manipulation, analysis, and reporting using SAS, generating datasets, and communicating with cross-functional teams.

Lead clinical studies by providing statistical support, employing advanced analytical methods, and collaborating with cross-functional teams to optimize clinical development processes.