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The Principal Biostatistician Consultant will oversee statistical aspects of drug development, provide statistical support, manage project timelines, mentor team members, and contribute to process improvements.

The Senior Statistical Programmer Consultant will manage programming tasks for clinical trials, oversee deliverables, and validate datasets while ensuring compliance with industry standards.

The Principal Biostatistician Consultant leads statistical methodologies and analysis for oncology clinical trials, contributing to regulatory submissions and collaborating with cross-functional teams.

The role involves leading statistical programming activities, mentoring programmers, overseeing clinical programming deliverables, and ensuring quality and compliance in regulatory submissions.

The Senior SDTM Programmer Consultant oversees SDTM deliverables for clinical project submissions, collaborating with teams and ensuring compliance with industry standards.

The Principal Statistical Programmer Consultant leads programming for oncology trials, ensuring programming quality and regulatory compliance while collaborating with various teams and managing timelines.

Lead and support statistical programming deliverables for clinical studies: implement protocol programming, ensure high-quality outputs and documentation, write/implement specifications, enforce standards and compliance, contribute best practices, manage tasks, communicate risks, and collaborate with statisticians, data managers, and study leads.

Lead statistical strategy and deliverables for Immunology clinical trials. Author and review SAPs, ADS, and clinical study report sections; review analysis outputs; collaborate with Clinical, Programming, Data Management, and Regulatory teams; mentor programmers; ensure FDA/ICH/GCP compliance.

Client-facing data scientist supporting clinical data transfer, ETL, validation, analysis, and Power BI dashboards. Build R scripts, assist data harmonization, support internal tools and basic web interfaces while working with cross-functional teams on clinical trial data.

Lead statistical programming strategy and teams for clinical studies, oversee development/validation of SDTM/ADaM datasets and TLFs, ensure regulatory submission readiness (eCTD), drive SAS/R workflows, automation, and cross-functional collaboration with biostatistics, data management, and regulatory teams.