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As a Principal Biostatistical Programmer, you will develop SAS programs for clinical trials, perform quality control, generate analysis datasets, and lead interactions with study teams.

Lead design, deployment, monitoring, and maintenance of server, VM, storage, and network infrastructure. Ensure regulatory compliance (e.g., 21 CFR Part 11), troubleshoot performance incidents, manage projects, update documentation, and recommend Data Center and infrastructure improvements.

As a Senior Project Manager, oversee project management tasks, budget adherence, client relations, and business development in the Neuroscience sector.

Administer and support finance systems (Workday, OneStream), manage user support requests, maintain and validate end-to-end data flows and integrations, develop report specifications, assist with system/UAT testing and month-end close, and support governance, documentation, and process standardization across finance systems.

As a Statistical Scientist Director, you will lead statistical strategies for client studies, develop innovative trial designs, manage projects, and communicate complex statistical concepts to stakeholders.

Lead statistical strategies for clinical trials, communicate with stakeholders, develop innovative trial designs, and advise on regulatory guidelines. Oversee statistical deliverables and manage project scope and budget while supporting business development.

Design, develop, and support enterprise AI solutions: lead AI solution design, build prompts/workflows, implement RAG, integrate AI platforms with corporate applications, deploy/manage AI services on Azure, administer Azure AI Foundry, troubleshoot tickets to SLA, and lead platform upgrades and documentation.

The Statistical Scientist Director will lead biostatistical strategies for complex studies, oversee projects, develop statistical deliverables, and provide regulatory guidance while managing client relationships and internal teams.

The Sr/Site Start up Associate II prepares and submits regulatory applications, negotiates site contracts, ensures compliance, and guides clinical trial processes.