Teams at Celerion

Leads multiple clinical research projects from initiation through closeout, managing scope, timelines, budgets, deliverables, risks, documentation, client relationships, and team coordination. The role serves as the primary client contact, drives communication and change management, monitors project and financial status, and supports client visits and facility tours.

Oversee end-to-end clinical data management for external site studies from startup through database lock. Responsibilities include managing EDC databases, designing and reviewing CRFs, conducting UAT, creating study documents, cleaning and reconciling data, managing queries, training site and client teams, coordinating stakeholders, communicating with sponsors, and ensuring regulatory compliance and timely final data delivery.

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.