ClinChoice Benefits Overview

Supports clinical trial statistical programming under senior guidance, including developing and validating datasets, tables, figures, listings, and CDISC-compliant regulatory submission deliverables. Uses SAS and/or R to process clinical data, contribute to SDTM and ADaM datasets, maintain specifications and documentation, perform quality checks, and resolve programming issues. Collaborates with biostatisticians, data managers, and cross-functional teams while developing expertise in clinical research standards and statistical programming.

Leads clinical pharmacology and PK/PD study design, protocol development, modeling and simulation, data analysis, regulatory reporting, and client collaboration. Uses pharmacokinetic software to support clinical trials, publications, and regulatory submissions. Provides scientific leadership, mentors junior pharmacologists, manages multiple projects, and applies current clinical pharmacology practices across pharmaceutical and biotechnology programs.

Supports clinical trial statistical activities under senior guidance, including study design and analysis, statistical analysis plans, tables, listings, figures, data checks, clinical study reports, documentation, and statistical programming collaboration. Works with cross-functional clinical research teams while following SOPs, regulatory requirements, and applicable standards such as CDISC, SDTM, and ADaM.