Scientist II, QSP/QST Consulting Services

Simulations Plus, Inc.; United States; A distancia; USD 110.000 - 150.000; Jornada completa

Descripción de la vacante

Simulations Plus, a global leader in model-informed and AI-accelerated drug development, seeks a Scientist II to execute consulting projects using QSP/QST models and MATLAB/THALES stack. Remote work is available with flexible schedules and a strong, supportive culture.

Responsibilities include building sub-models, translating PD/MoA data to model parameters, and leading project activities while advancing R&D efforts in QST liver injury modeling. Travel as needed.

Formación

• 2+ years of QSP/QST modeling experience or demonstration of the equivalent skill sets
• Proficiency in mathematics, dynamic systems, drug development
• General knowledge of relevant therapeutic areas, including clinical endpoints and underlying biology
• 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
• Maintains a positive attitude while interacting with colleagues and clients
• Must be able to multitask and have good organizational skills
• Self-motivated with ability to work with minimal supervision
• Occasional travel for conferences, meetings, and training

Responsabilidades

• Design, write, test, and use computer code to build and maintain the sub-model(s), representing core cellular, molecular, and/or biochemical processes in a given model
• Represent compound pharmacodynamics (PD) and/or mechanism of action (MoA), including translating laboratory data into model parameters and curation of clinical data for calibration/validation
• Learn and effectively utilize company agentic AI solutions for technical work
• Contribute to the activities required for successful completion of all goals within consulting projects
• Contribute (as time allows) to R&D efforts, including updating the “license-ready” versions of the various models and supporting ongoing development of QST models of liver injury (i.e., the DILI-sim consortium)
• Combine technical and project management work, including components such as systems pharmacology modeling, software code development, and maintenance in designated software environments
• Develop plans to complete all tasks and provide all deliverables within a time frame consistent with the services agreement signed with the sponsor
• Schedule the necessary meetings including internal and external collaborators
• Exert leadership in the areas of presentation and report preparation by exhibiting strong skills for effective presentations and reports, applying diligent scientific review, and being timely with execution and responses to feedback
• Lead consulting projects, upon demonstrating the necessary technical and project management skills and availability of a suitable project
• Participate in preparation and review of joint manuscripts between the company and the sponsor
• Manage the effort expended for a given project to remain consistent with the resources allocated for the project per the signed contract
• Publish work in scientific journals, with minimal review required by their supervisor, including documentation preparation, text development, figure development, and correspondence with editors and peer reviewers
• Train others on QSP/QST and the various models
• Other duties as assigned

Conocimientos

QSP/QST modeling

Mathematics & dynamic systems

Communication skills

Self-motivated

Educación

Master's degree in pharmaceutical science or biomedical engineering

PhD in pharmaceutical science or biomedical engineering (preferred)

Herramientas

MATLAB

THALES

Julia

SimBiology

Monolix

GastroPlus

C++ programming

Descripción del empleo

Simulations Plus stands as a global leader in model-informed and AI-accelerated drug development. We create value for our clients by accelerating the discovery, development, and commercialization of pharmaceuticals and other products through innovative science-based software and consulting solutions.

Leadership truly cares about maintaining a positive culture and employee well-being. We offer fully remote work, flexible schedules, and generous vacation policy along with affordable health coverage, annual bonus, and more! Check out how much our employees love working here: https://www.comparably.com/companies/simulations-plus .

The Scientist II will contribute to the technical execution of consulting projects using Quantitative Systems Pharmacology (QSP) and/or Toxicology (QST) models and methodologies. Frequently, consulting projects are conducted in Simulations Plus models, leveraging technical expertise in MATLAB or THALES.

Other work can include technical expertise in SimBiology, Julia, Monolix, as well as script generation using MATLAB, R, Python, etc. Consulting projects also leverage knowledge of multiple therapeutic areas including oncology, hepatology, metabolic diseases, pulmonary diseases, and inflammatory and immune diseases, as well as adverse events (e.g., liver injury, lung injury, cytopenias, cytokine release syndrome).

Department: Strategic Consulting Services/Quantitative Systems Pharmacology

Internal Grade: 12

Direct Reports: No

Status: Exempt

Location: Remote

Job Responsibilities

• Design, write, test, and use computer code to build and maintain the sub-model(s), representing core cellular, molecular, and/or biochemical processes in a given model
• Represent compound pharmacodynamics (PD) and/or mechanism of action (MoA), including translating laboratory data into model parameters and curation of clinical data for calibration/validation
• Learn and effectively utilize company agentic AI solutions for technical work
• Contribute to the activities required for successful completion of all goals within consulting projects
• Contribute (as time allows) to R&D efforts, including updating the “license-ready” versions of the various models and supporting ongoing development of QST models of liver injury (i.e., the DILI-sim consortium)
• Combine technical and project management work, including components such as systems pharmacology modeling, software code development, and maintenance in designated software environments
• Develop plans to complete all tasks and provide all deliverables within a time frame consistent with the services agreement signed with the sponsor
• Schedule the necessary meetings including internal and external collaborators
• Exert leadership in the areas of presentation and report preparation by exhibiting strong skills for effective presentations and reports, applying diligent scientific review, and being timely with execution and responses to feedback
• Lead consulting projects, upon demonstrating the necessary technical and project management skills and availability of a suitable project
• Participate in preparation and review of joint manuscripts between the company and the sponsor
• Manage the effort expended for a given project to remain consistent with the resources allocated for the project per the signed contract
• Publish work in scientific journals, with minimal review required by their supervisor, including documentation preparation, text development, figure development, and correspondence with editors and peer reviewers
• Train others on QSP/QST and the various models
• Other duties as assigned

Qualifications

• 2+ years of QSP/QST modeling experience or demonstration of the equivalent skill sets
• Proficiency in mathematics, dynamic systems, drug development
• General knowledge of relevant therapeutic areas, including 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
• Maintains a positive attitude while interacting with colleagues and clients
• Must be able to multitask and have good organizational skills
• Self-motivated with ability to work with minimal supervision
• Occasional travel for conferences, meetings, and training

Education

• Master’s degree in pharmaceutical science, biomedical engineering, or related field
• PhD in pharmaceutical science, biomedical engineering, or related field preferred