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Planet Pharma Group

Senior Research Associate DMPK (P3553)

Pay: Not specified

Posted: 2 weeks ago

Location: Redwood City, CA (Onsite)

Last Updated: 1 week ago

Hours: Full-Time

Expires: 10/4/2026

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What they do

A Research Associate typically has more experience than a Research Assistant. Responsibilities can include the planning and design of research projects, conducting experiments, analyzing data, contributing to research publications or grant proposals, and collaborating with other researchers. Works in a variety of fields within science or the social sciences, in programs based at a university or research institution, or works on government or industry sponsored research projects. Conducts field or library research or recruits participants for a study; may also assist with legal research. These roles are often held by people with advanced degrees in their field of study with several years of experience in research or academia.

$77,239 / year median in California

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Job Description

Senior Research Associate DMPK The Opportunity:

Develop

LC-MS/MS

methods and analyze in vivo and in vitro samples to support ADME, pharmacokinetic, and toxicokinetic studies, etc. Handle a variety of tissues, including tumors, from tissue homogenization through sample preparation for bioanalysis. Perform data analysis, prepare experimental result reports, and upload data to electronic notebooks. Conduct in vitro

ADME/DMPK

assays in biological matrices, including hepatocytes, microsomes, blood, and plasma, ect. Support laboratory operations, including

LC-MS/MS

instrument maintenance and troubleshooting.

Required Skills, Experience and Education:

Bachelor's or master's degree in pharmaceutical sciences or a related scientific discipline, with 5+ years of industry experience for bachelor's degree holders or 3+ years for master's degree holders. Hands-on experience in operating and maintaining

LC-MS/MS

systems. Hands-on experience in

LC-MS/MS

method development and bioanalytical analysis. Knowledge of biological sample preparation and extraction techniques for downstream

LC-MS/MS

analysis. Hands-on experience in

HPLC/UPLC

method development. Ability to customize and follow established assay protocols. Ability to manage multiple laboratory and project tasks efficiently. Ability to work effectively in a flexible, team-oriented environment. Highly organized and detail-oriented, with excellent recordkeeping skills and the ability to adapt to a dynamic, fast-paced environment.

Preferred Skills:

Previous hands-on experience in SCIEX QTRAP and Thermo Q Exactive mass spectrometers. Previous hands-on experiences on bioanalytical method development in compliance with regulatory requirements. Working experience in DMPK lab.