Senior/ Principal Scientist/ Senior Principal – PBPK and Pharmacometrics, M at Genentech
San Francisco, CA 94015, USA -
Full Time


Start Date

Immediate

Expiry Date

28 Nov, 25

Salary

318200.0

Posted On

28 Aug, 25

Experience

3 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

No

Skills

Good communication skills

Industry

Pharmaceuticals

Description

THE POSITION

We advance science so that we all have more time with the people we love.
The Clinical Pharmacology Department at Genentech, Inc. is seeking Ph.D. level Senior Scientist, Principal Scientist, or Senior Principal Scientist who is driven to use cutting edge modeling approaches to advance the clinical development of novel drug candidates to join our diverse group of pharmacometricians, system modelers (PBPK or QSP), advanced programmers, artificial intelligence/machine learning scientists, and clinical pharmacologists. This individual will be responsible for the development and implementation of Clinical Pharmacology (Clin Pharm) and/or Modeling & Simulation (M&S) strategy, in order to ensure that the right drug is administered to the right patient at the right dose via the right route. Physiologically-based Pharmacokinetic (PBPK) modeling will be a key focus of this position. Key technical responsibilities are to strategize, plan, execute, and report PBPK M&S independently, as well as to present work at cross-functional teams, department meetings, senior management review committees, regulatory interactions, and scientific conferences. A qualified candidate could be responsible for Clin Pharm strategy/support such as leading the design, conduct, and reporting of Clin Pharm studies, as well as other M&S strategy/support such as population PK/PD models, disease models, statistical models, quantitative system pharmacology (QSP) models, clinical trial simulations, literature meta-analysis, machine learning/deep learning. Other responsibilities may include planning, writing, and reviewing relevant clinical documents such as study protocols, analysis plans, reports, and regulatory documents. These will be accomplished by working in close partnership with other scientists in Clinical Pharmacology, Clinical Science, Biostatistics, Translational PKPD, DMPK, Translational Safety, Biomarker, Diagnostics, Regulatory, RWD (Real World Data), and other functions on project teams. The successful candidate should be a forward thinking scientist capable of working effectively across diverse regions, cultures, and time zones, creating an environment of belonging and inclusion.

Responsibilities

Please refer the Job description for details

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