31 data-science Fellowship positions at Center for Drug Evaluation and Research (CDER)

FDA Fellowship in Risk-Based Assessment & Inspections

*Applications will be reviewed on a rolling-basis. FDA Office and Location: A research opportunity is available in the Office of Strategic Programs/Office of Business Informatics, Center for Drug

FDA Predictive Analytics Fellowship

high volume of structured and unstructured data related to regulated facilities and products and has limited resources to perform manual reviews. Through applying modern statistical approaches, such as

FDA Fellowship in Program, Policy and Operational Analysis

data need identified by the mentor, participate in the development of research methodology and project planning through contributing to relevant research, compile and analyze relevant qualitative and

FDA Modeling and Simulation Fellowships

) provides expertise in advanced quantitative methods for the generic drug research program and conducts regulatory science and research activities based on quantitative approaches. Some of the

FDA Research Fellowship in Over-the-Counter Spray Drug Product

Permanent Residents (LPR), and foreign nationals. Non-U.S. citizen applicants should refer to the Guidelines for Non-U.S. Citizens Details page  of the program website for information about the valid

FDA Oligonucleotide Research Fellowship

, the participant will participate in data evaluation and documentation, collaborating with their mentor on publications, presentations, or reports to learn effective communication of regulatory science to both

FDA Postdoctoral Glyco-technology Lab Fellowship

for information about the valid immigration statuses that are acceptable for program participation. This program, administered by ORAU through its contract with the U.S. Department of Energy to manage the Oak Ridge

FDA Epidemiology to Enhance Safety Surveillance Fellowship

: The participant will gain knowledge with using data from a nationally representative survey, describe the prevalence of use, misuse, and use disorders involving certain substances of interest, nationally and within

FDA Bioequivalence of Complex Generic Products Fellowship

Permanent Residents (LPR), and foreign nationals. Non-U.S. citizen applicants should refer to the Guidelines for Non-U.S. Citizens Details page  of the program website for information about the valid

FDA Fellowship in Biomarker Use in Rare Disease Drug Development

will review rare disease medical product applications for previously approved products to characterize the use and key elements of biomarkers in addition to gathering data on disease characteristics