Scientist II, QSP/QST Consulting Services

Simulations Plus, Inc.

. Design, write, test, and use computer code to build and maintain sub-models representing cellular, molecular, and/or biochemical processes .

Posted 10/10/2026full-timeRemote • United StatesJuniorMid-Level💰 $110,000 - $130,000 per yearWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in QSP/QST modeling, drug development, and systems pharmacology, with proficiency in MATLAB, THALES, and C++ programming. Capable of leading consulting projects, managing deliverables, and effectively communicating scientific findings.

Highest-signal resume keywords

QSP/QST Modeling ExperienceMATLAB ProficiencyC++ ProgrammingStrong Verbal And Written Communication SkillsProject Management

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

QSP/QST ModelingMATLABC++ ProgrammingDynamic SystemsDrug DevelopmentPBPK ModelingPKPD ModelingSimBiologyMonolixGastroPlus™

Soft Skills

Strong Verbal CommunicationStrong Written CommunicationMultitaskingOrganizational SkillsSelf-Motivated

Tools & Technologies

THALESMATLABSimBiologyMonolixGastroPlus™

Certifications & Qualifications

Master’s Degree In Pharmaceutical SciencePhD In Pharmaceutical Science

Industry Keywords

PharmacodynamicsCellular BiologyMolecular BiologyBiochemistryClinical Endpoints

Tech Stack

Tools & technologies

C++

About the role

Key responsibilities & impact

Design, write, test, and use computer code to build and maintain sub-models representing cellular, molecular, and/or biochemical processes
Represent compound pharmacodynamics and/or mechanism of action, translating laboratory data into model parameters and curating clinical data for calibration and validation
Learn and utilize company agentic AI solutions for technical work
Contribute to successful completion of consulting project goals
Contribute to R&D efforts, including license-ready model updates and development of QST models of liver injury
Combine systems pharmacology modeling, software code development, maintenance, and project management
Develop plans and deliverables consistent with sponsor service agreements
Schedule meetings with internal and external collaborators
Prepare presentations and reports, conduct scientific review, and respond to feedback
Lead consulting projects when qualified and available
Participate in preparation and review of joint manuscripts
Manage project effort within contracted resources
Publish scientific work, including documentation, figures, and correspondence with editors and peer reviewers
Train others on QSP/QST and related models
Perform other duties as assigned

Requirements

What you’ll need

2+ years of QSP/QST modeling experience or equivalent skill sets
Proficiency in mathematics, dynamic systems, and drug development
General knowledge of relevant therapeutic areas, clinical endpoints, and underlying cell and molecular biology and/or biochemistry
Experience with MATLAB, THALES, Julia, SimBiology, Monolix, GastroPlus™, and/or C++ programming
Experience with PBPK, PK, popPK, and/or PKPD modeling
Basic familiarity with large-language models and agentic AI
Understanding of how to apply modeling and simulation for maximum impact
Strong verbal and written communication skills
Ability to multitask and good organizational skills
Self-motivated with ability to work with minimal supervision
Occasional travel for conferences, meetings, and training
Master’s degree in pharmaceutical science, biomedical engineering, or related field required
PhD in pharmaceutical science, biomedical engineering, or related field preferred

Benefits

Comp & perks

Fully remote work
Flexible schedules
Generous vacation policy
Affordable health coverage
Annual bonus
Employee well-being programs
Opportunities to publish work in scientific journals
Professional training and development opportunities