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FDA Data Mining in Cardiovascular Safety Model Development U.S. Food and Drug Administration (FDA) in United States
Degree Level
Postdoc
Field of study
Computer Science
Funding
Monthly stipend commensurate with educational level and experience; appointment initially for one year and renewable contingent on funds.
Deadline
Nov 20, 2026
Country
United States
University
US Food and Drug Administration
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About this position
This research opportunity is based at the U.S. Food and Drug Administration (FDA) in the Office of Translational Sciences, Office of Clinical Pharmacology, Division of Applied Regulatory Science within CDER in Silver Spring, Maryland.
The project focuses on data mining and database development for cardiovascular safety, supporting regulatory science through systematic analysis of nonclinical and clinical cardiotoxicity information. The selected researcher will help build and curate comprehensive databases to assess the current landscape of cardiovascular safety data used in drug development and regulatory decision-making.
Work will include applying advanced data mining techniques, statistical modeling, and computational tools to identify patterns, gaps, and trends in large datasets relevant to cardiac safety. These datasets include human induced pluripotent stem cell-derived cardiomyocyte (hiPSC-CM) data, ion channel pharmacology, in vivo and clinical QT data, and other cardiotoxicity endpoints.
The position offers collaboration with FDA scientists on how real-world and experimental data can be integrated to inform translational regulatory strategies and improve cardiovascular safety assessment. The research environment includes engagement with internal FDA scientists and regulators, external academic researchers, and industry stakeholders, with opportunities to present findings and contribute to scientific manuscripts.
The mentor for this opportunity is Tromondae Feaster.
Funding details
Monthly stipend commensurate with educational level and experience; appointment initially for one year and renewable contingent on funds.
What's required
The qualified candidate should be currently pursuing or have received a doctoral degree in a relevant field. Applicants must submit an application, transcripts, a current resume/CV with academic history, employment history, relevant experiences, and publication list, and one educational or professional recommendation. All documents must be in English or include an official English translation. U.S. citizens, lawful permanent residents, and foreign nationals may apply, but non-U.S. citizens must meet the program’s valid immigration status requirements and background investigation rules; proof of health insurance is required, and the OPM background investigation can only be completed for individuals who have resided in the U.S. for a total of three of the past five years.
How to apply
Go to the opportunity page and scroll to the bottom, then click APPLY. Prepare an application, transcripts, CV, and one recommendation before submitting. If you have questions, email [email protected] and include the reference code FDA-CDER-2026-0160.
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Make your next move.
Prepare your application
Review drafts and confirm requirements with the university.