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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.

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.

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.

The Senior/Principal Statistical Programmer develops programming code for statistical analysis, ensures output quality, manages project documentation, and leads programming activities while mentoring junior staff.

The role requires a Senior Statistical Programmer with expertise in R and R Shiny to create visualizations and work with clinical trial data, alongside managing multiple studies and effective communication.

The Sr Biostatistician will be responsible for statistical activities including SAP writing, mock shell creation, CSR review, and will need proficiency in R and SAS with experience in clinical trials and therapeutic areas.

The Project Specialist at Syneos Health will collaborate on biopharmaceutical projects, support customer success, and contribute to clinical development initiatives within a diverse team.