50 parallel-and-distributed-computing-phd Fellowship positions at Center for Drug Evaluation and Research (CDER)

FDA Fellowship - Inactive Ingredient (IID) Program operated by OB

Center for Drug Evaluation and Research (CDER) | Southern Md Facility, Maryland | United States | about 3 hours ago

therapeutics and generic drugs. These efforts cover more than just medicines. Research Project: The Inactive Ingredients Database (IID) program within the FDA's Center for Drug Evaluation and Research (CDER

FDA Fellowship - Computational Toxicology

Center for Drug Evaluation and Research (CDER) | Silver Spring, Maryland | United States | about 3 hours ago

stakeholders. Learning Objectives: Under the guidance of a mentor, you will learn about the development of computational models for regulatory use. Your fellowship research and training activities may include

FDA Computational Biology and Pharmacology Fellowship

Center for Drug Evaluation and Research (CDER) | Silver Spring, Maryland | United States | about 3 hours ago

developing comprehensive toxicology databases and computational models by analyzing proprietary data from drug applications, as well as public literature data, focusing on endpoints where New Approach

FDA Fellowship in Statistical Methods for New Approach Methodologies (NAMs)

Center for Drug Evaluation and Research (CDER) | Silver Spring, Maryland | United States | about 3 hours ago

statistical methods for evaluating parallelism of dose-response curves between test and reference standards through simulation studies. Evaluation of multiple statistical approaches — including logistic

FDA Fellowship - Office of Pharmaceutical Quality (OPQ) Initiative - Data Analysis

Center for Drug Evaluation and Research (CDER) | Silver Spring, Maryland | United States | about 3 hours ago

algorithm performance. You will analyze assignment data from December 2025 to the present to identify workload distribution patterns and refine the algorithm using mathematical modeling, programming, and

FDA Fellowship RLD vs. Generic Buprenorphine Films: A Physicochemical Study of Equivalence & Manipulability

Center for Drug Evaluation and Research (CDER) | Saint Louis, Missouri | United States | about 3 hours ago

between formulation microstructure, chemical distribution, material properties, and product performance. Gain exposure to regulatory science and complex drug-product evaluation, including how advanced

FDA Fellowship in Regulatory Science Advancement for Continuous Glucose Monitoring (CGM) Endpoints

Center for Drug Evaluation and Research (CDER) | Silver Spring, Maryland | United States | about 3 hours ago

statistical approaches for handling complex, hierarchical CGM data under combined missingness and censoring scenarios, extend these methodologies beyond TIR to metrics with distinct distributional

FDA Fellowship in Regulatory Science Advancement for Continuous Glucose Monitoring (CGM) Endpoints

Center for Drug Evaluation and Research (CDER) | Silver Spring, Maryland | United States | about 3 hours ago

statistical approaches for handling complex, hierarchical CGM data under combined missingness and censoring scenarios, extend these methodologies beyond TIR to metrics with distinct distributional

FDA Fellowship - Office of Pharmaceutical Quality (OPQ) Assignment Management Initiative - Data Analysis

Center for Drug Evaluation and Research (CDER) | Silver Spring, Maryland | United States | 2 months ago

algorithm performance. You will analyze assignment data from December 2025 to the present to identify workload distribution patterns and refine the algorithm using mathematical modeling, programming, and

FDA Fellowship in Quantitative Regulatory Science: Integrating Nonclinical and Clinical Data to Support Targeted Therapy Development

Center for Drug Evaluation and Research (CDER) | Silver Spring, Maryland | United States | about 3 hours ago

structured learning opportunities in regulatory science and computational modeling applications in drug development and use of artificial intelligence for data mining. You will gain experience in regulatory