We would like to announce a position in the Clinical Pharmacology Modelling and
Simulation (CPMS) group of GlaxoSmithKline (GSK) Research and Development (R&D)
China. Established in 2007 as an end-to-end R&D centre, GSK China has enjoyed
tremendous growth and built a strong R&D infrastructure and pipeline with main
focus on neurological diseases. As a member of our global department, you have
the opportunity to shape drug development programs by applying cutting-edge
sciences and methodologies.
The position is based in Shanghai, a dynamic and vibrant city. The following
are the responsibilities and qualifications for the position. Please send your
CV to [email protected]<mailto:[email protected]> if you are interested.
Sincerely,
Peiming Ma
Responsibilities
* Use clinical pharmacology (CP) principles and modelling & simulation
(M&S) methods to support research and development decisions for compounds from
pre-candidate selection through post-licensing stages (e.g. investigation of
target mechanisms, design and dose selection of PK-PD studies, population PK-PD
analysis, disease-progression modelling, simulation-assisted trial design,
therapeutic dose recommendation).
* Design CP strategies for drug projects; represent CPMS on the local
project/study teams for all R&D activities (e.g., planning and reporting of CP
studies, health authority dialogues, and writing the relevant components of
regulatory documents).
* Effectively represent the CPMS department on internal teams and to
external groups; contribute to CPMS global department science via participation
of learning activities, scientific sharing, presentations and publications.
Qualifications
* A doctoral degree in PK or other quantitative sciences, and preferably
drug industry experience.
* Experience in PK-PD modelling and simulation analysis, data
interpretation, and report writing; proficiency in using modelling and
simulation software such as R, Monolix, NONMEM, and WinNonlin, etc.
* Excellent communication skills and drive to achieve results; ability
to work independently and prioritize assignments with minimal supervision, and
foster effective relationships with interdisciplinary teams for collaboration.
* Good knowledge of life sciences, pharmacology, statistics, drug R&D
processes and global/local regulatory requirements in pharmacology-related
areas.