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US Food and Drug Administration

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FDA Modeling and Simulation Fellowships U.S. Food and Drug Administration (FDA) in United States

Degree Level

Master's

Field of study

Computer Science

Funding

Monthly stipend commensurate with educational level and experience; appointment initially for one year and may be renewed subject to FDA recommendation and availability of funds.

Deadline

Mar 30, 2027

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Country

United States

University

US Food and Drug Administration

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Keywords

Computer Science
Biomedical Engineering
Mathematics
Artificial Intelligence
Medical Science
Pharmacy
Regulatory Science
Bioequivalence
Computational Modelling
Statistics
Pharmacokinetic
Pharmacodynamic
Physics
Large Language Models
ML

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About this position

This fellowship is based in the Division of Quantitative Methods and Modeling within the FDA’s Center for Drug Evaluation and Research in Silver Spring, Maryland. The group works on regulatory science and quantitative research that supports the development and review of generic drugs, with a strong emphasis on modeling, simulation, data analysis, and data mining for public health decision-making.

Participants will join research activities spanning a wide range of modern quantitative approaches for drug evaluation. The project highlights modeling and simulation for solid oral products, bioequivalence assessment, and biowaivers, as well as mechanistic and data-driven approaches for complex generic products. The work also includes population pharmacokinetics, PK/PD modeling, clinical trial simulation, and methods development for locally acting products administered by non-oral routes.

The fellowship also offers opportunities to work on computational methods that improve FDA review efficiency and scientific infrastructure. Areas mentioned include scientific computing, data infrastructure, analysis tools, artificial intelligence, machine learning, large language models, and integration of these tools with conventional pharmacokinetic modeling. The environment is described as fast-paced and collaborative, with senior researchers focused on advancing quantitative methods for generic drug regulation.

The mentor for this opportunity is Andrew Babiskin.

Funding details

Monthly stipend commensurate with educational level and experience; appointment initially for one year and may be renewed subject to FDA recommendation and availability of funds.

What's required

The candidate should be currently pursuing or have received a master's or doctoral degree in one of the relevant fields, and the degree must have been received within five years of the appointment start date. Applicants must submit an application, transcripts, a current resume/CV with academic and employment history, relevant experience, and publication list, and one educational or professional recommendation. All documents must be in English or include an official English translation. This opportunity is open to U.S. citizens, lawful permanent residents, and foreign nationals, and non-U.S. citizens must meet the program's acceptable immigration-status guidelines. Proof of health insurance is required, and an applicant must be able to pass a successful background investigation; OPM can complete the investigation only for individuals who have resided in the United States for a total of three of the past five years.

How to apply

Apply through the Zintellect opportunity page by scrolling to the bottom and clicking APPLY. Prepare the application, transcripts, current CV/resume, and one recommendation letter. If you have questions, email [email protected] and include the reference code FDA-CDER-2026-0011.

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