PK Scientist
Core
Senior Clinical Pharmacology professional supporting protocol development and PK/PD analysis across Phase I–IV clinical trials.
Role type
Senior PK Scientist
Builds
Clinical Study Reports (CSRs) and clinical pharmacology trial protocols
Domain
Clinical Pharmacology / Drug Development
Deliverable
production ML models | product features | dashboards & analysis | research | client delivery | infrastructure | physical/clinical work
Required skills
Non-compartmental analysis (NCA), Clinical Pharmacology Analysis Plan (CPAP) development, PK/PD analysis, Protocol writing, Data handling, Regulatory compliance (ICH-GCP), QC review
Preferred skills
R programming
Technologies
Phoenix WinNonlin, R
Responsibilities
Author and coordinate development of clinical pharmacology trial protocols, Perform preliminary, interim, and final PK, PD, and PK/PD analyses, Develop the Clinical Pharmacology Analysis Plan (CPAP) and generate data handling logbooks, Create tables, listings, and figures for Clinical Study Reports, Conduct QC review of protocols, analyses, datasets, and all deliverables
Seniority
Senior, hands-on IC
