Teams at Celerion

Performs pharmacokinetic data analysis, PK and PD interpretation, quality control reviews, clinical report writing, regulatory filing preparation, and study documentation management. The scientist independently conducts PK analyses, supports client interactions, prepares internal presentations, and interprets statistical findings. The role requires collaboration with senior scientists and may involve nonlinear mixed-effects or physiologically based pharmacokinetic modeling.

Performs pharmacokinetic and pharmacodynamic data analyses, independently interprets PK and statistical results, conducts quality-control reviews, writes clinical reports, prepares regulatory submission files, maintains study documentation, and supports client interactions and internal presentations.

Build and administer EDC trials including eCRF design and EDC builds, program edit checks, create test data and environments, execute UAT coordination, program reports/listings with Veeva CDB, manage secure data imports, validate system upgrades, and maintain CDISC database standards.