The Clinical Pharmacology Review Team for Metabolic and Endocrine Drug Products
at CDER, FDA is looking for a post-doctoral fellow to work on internal research
projects in clinical pharmacology. These projects have potential to influence
the design of future clinical studies, methodology used for data analysis for
drug approval, and class labeling. This is a good opportunity for applicants to
gain expertise in quantitative clinical pharmacology and drug development by
working with leading scientists at FDA.
We are looking for a candidate preferably with the following skills:
1. Holds a Ph.D. degree in clinical pharmacology, pharmacometrics, or related
disciplines
2. Working knowledge of pharmacokinetic-pharmacodynamic modeling and basic
statistics
3. Hands-on-experience on software routinely used in modeling and simulation
such as NONMEM, WinNonLin, SAS, S-plus, R and JMP
4. Experience in longitudinal data analysis, time-to-event or adverse event
analysis is a plus
5. Excellent communication and time-management skills
This is a one year fellowship. The applicant should be a U.S. citizen or
permanent resident. The appointment is for one year, which may be renewed based
on project needs and priorities. The participant will receive a monthly stipend
commensurate with his/her educational level and work experience. The
participant must show a proof of medical insurance. The participant will work
full time at FDA site in Silver Spring, Maryland. However, participant does not
become employee of FDA or the project administrator, and there are no fringe
benefits paid.
Interested candidates are encouraged to send their CV to
[email protected] and [email protected]