Teams at Celerion

Perform scheduled clinical trial procedures under study protocols, including vital signs, ECGs, blood draws, telemetry monitoring, participant care, documentation, and adverse-event reporting. Collaborate with study managers to support successful overnight trials involving healthy participants. The role requires a current Nebraska RN or LPN license, clinical assessment skills, and strong computer and documentation abilities. ACLS certification is preferred. Overnight shifts run approximately 7 p.m. to 7:30 a.m., including one weekend per month.

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.