Research Scientist

Vedi l’offerta su Go Lavoro: golavoro.it/annuncio-lavoro/7b8308

Experteer Overview In this Senior PK Scientist role, you will support protocol development and PK/PD analyses across clinical trial phases. You will work within a cross‐functional, regulated development environment to contribute to CPAPs, analyze data, and draft clinical pharmacology sections of CSRs. Your work will emphasize non‐compartmental PK methods, data handling, and quality control to ensure regulatory compliance. The position offers exposure to global trials and a chance to shape pharmacology strategy in a leading CRO setting. You'll operate at the intersection of science, data, and regulatory standards to drive robust clinical pharmacology outcomes.
Retribuzione / Benefits Author and coordinate development of clinical pharmacology trial protocols and manage approval processes
Perform PK, PD, and PK/PD analyses using non‐compartmental methods across study phases
Develop the CPAP and data handling logbooks prior to final NCA
Create tables, listings,



and figures and contribute to drafting clinical pharmacology sections of CSRs
QC review protocols, analyses, datasets, and deliverables to ensure SOP, ICH‐GCP, and regulatory compliance
Responsabilità 4+ years of relevant clinical pharmacology experience
Bachelor's degree or higher in a scientific discipline
Hands‐on PK & PD software knowledge, especially Phoenix WinNonlin; working knowledge of R for PK/PD (advantage)
Excellent data‐handling skills and knowledge of database structuresli

Experience with noncompartmental PK analysis and PK/PD analyses
Strong written and verbal communication skills
Requisiti fondamentali annual leave entitlements
health insurance offerings
retirement planning
Global Employee Assistance Programme
life assurance
flexible country-specific optional benefits #J-18808-Ljbffr

Vedi l’offerta su Go Lavoro: golavoro.it/annuncio-lavoro/7b8308