Jobs at Celerion

Conduct statistical analyses for clinical research studies using SAS. Responsibilities include developing statistical analysis plans, generating randomization schedules, preparing tables, figures, listings, and reports, interpreting data, supporting database transmissions, reviewing deliverables, assisting with programming, and coordinating with internal teams and clients.

Lead national business development for biologics, biomarkers, molecular and cellular bioanalysis services. Acquire new biotechnology and pharmaceutical clients, build opportunity pipelines, develop scientific and commercial relationships, lead proposals and negotiations, and support growth of bioanalytical laboratories. Provide technical expertise in advanced assay technologies and emerging therapeutic modalities while collaborating with scientific, operational, marketing, and regional business development teams.

Manages preparation, review, negotiation, execution, and tracking of client and subcontractor agreements for clinical research projects. Coordinates legal review and works with Finance, Operations, Business Development, sponsors, subcontractors, and other stakeholders. Develops change orders, payment schedules, and cash flow analyses while assessing contractual business risk and supporting high-volume contract activity.

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.

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.