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The Senior Clinical Programmer is responsible for programming, testing database designs, managing reporting tools, troubleshooting issues, and collaborating with teams to ensure compliance and data integrity in clinical programming tasks.

The Principal Biostatistician in Clinical Pharmacology will lead statistical aspects of clinical studies, contribute to research design, and collaborate with teams to ensure drug development success.

The Senior Statistical Programmer develops programming codes using SAS for data analysis, leads programming activities, ensures quality standards, and manages project documentation and timelines, while mentoring junior programmers and communicating with various stakeholders.

The role involves programming using SAS and R, developing statistical outputs, managing project documentation, mentoring staff, and acting as the lead programmer for PK analysis in clinical trials.

The Principal Stat Programmer develops custom SAS code for clinical studies, ensuring quality outputs, managing project timelines, mentoring junior staff, and collaborating with project teams on clinical data analysis.

Lead statistical programming tasks including developing custom code using SAS, ensuring output quality, and mentoring junior programmers. Manage multiple projects, maintain documentation, and engage in sponsor meetings.

The Clinical Scientific Advisor supports clinical trial activities, builds relationships with KOLs, and ensures protocol execution. Requires 2+ years in clinical research, preferably in Neuroscience/Psychiatry.

The Sr Statistical Programmer develops programming code to generate datasets and graphical outputs, ensuring quality and compliance with specifications. They lead programming activities, manage project timelines, and mentor junior staff, while facilitating effective communication and documentation throughout the project lifecycle.

Provide statistical support for clinical trials, prepare analysis plans, review programming specifications, coordinate biostatistics activities, and manage project deliverables.

Lead and support statistical activities across clinical trial lifecycles: prepare SAPs, review CRFs and database design, coordinate biostatistics and programming work, perform QC, support regulatory interactions, mentor staff, and contribute to proposals and study reporting.