Plans, designs, implements and analyzes routine Pharmacometrics (PMx) studies to advance scientific knowledge, in collaboration with other team members.
Performs analyses such as NCA, compartmental modeling, PopPK, translational modelling, disease modelling, Pop PK/PD, E-R analyses to deliver PMx results, interpretation and discussion.
Collaborates with Scientific Writing to ensure TFLs for PMx reports are complete.
Works in conjunction with Scientific Writing, Quality Control and QAA to issue study reports in support of IND/CTA submissions and other regulatory documents.
Contributes to preparation of PMx materials for regulatory background packages, e.g. for pre-IND, EOP2, and pre-BLA meetings.
Is highly skilled in use of relevant software, including MS-Excel, R, R-Studio, Prism, Phoenix WinNonlin, NLME, STAN and NonMem, working in department computing environment to perform advanced PMx analyses.

A PhD in Biology, Pharmacology, Engineering or a Pharmacy (Pharm.D.), Medicine (MD) degree
3+ years of relevant Clinical Pharmacology experience
Able to communicate effectively with and influence team members from other functions.
Fully understand processes and are able to represent PMx on process initiatives.

Senior Clinical Pharmacologist

Key skills