U.S. Food and Drug Administration (FDA) Regulatory Analysis of Dose-Finding and Optimization Approaches in Targeted Oncology Therapeutics
Full-time ORISE research appointment at FDA CDER to collect and analyze dose-selection and optimization strategies used for targeted oncology therapeutics (e.g., TKIs) by extracting data from NDAs, BLAs, and INDs and evaluating dose-finding methods and exposure-response relationships. The role includes data analysis, presenting findings to clinical pharmacology leadership, and contributing to …
Source
Dates
Eligibility
Keywords
Supporting Links
Documents
Similar Opportunities
-
U.S. Food and Drug Administration (FDA) Product Specific Guidance and Research Fellowship
U.S. Food and Drug Administration
-
U.S. Food and Drug Administration (FDA) In Vitro and In Vivo Bioequivalence Fellowship
U.S. Food and Drug Administration
-
Postdoctoral Research Fellowships in Biology (PRFB)
National Science Foundation
-
DoW Peer Reviewed Cancer, Clinical Trial Award
Dept. of the Army -- USAMRAA
-
Translational Neural Devices (R61/R33 - Clinical Trial Optional)
National Institutes of Health ▸ National Institute of Neurological Disorders and Stroke
Find tens of thousands more opportunities — free
Scout accounts are free. Sign up to browse the full funding database, unlock the solicitation links and documents for this opportunity, and see how well each one fits your organization.
-
Tens of thousands of funding opportunities
Search and filter every grant and solicitation in Scout — all free, no credit card required.
-
Instant Fit Analysis
Let our grant expert AI score how well this opportunity aligns with your organization, strengths, gaps, and how to improve your chances of winning funding.
-
Source links & full documents
Jump straight to the solicitation and download every attachment.
-
Save opportunities & track deadlines
Keep the opportunities that fit in one place and stay ahead of every due date.
Already have an account? Sign In
Trusted by 500+ Happy Customers