ORISE Fellow Positions available within the Food and Drug Administration (FDA)
Modeling and Simulation Positions at FDA
Position Description:
The Division of Quantitative Methods and Modeling
(DQMM) in the Office of Research and Standards (ORS) within the Office of
Generic Drugs (OGD) of the Food and Drug Administration has Oak Ridge Institute
for Science (ORISE) fellow positions available.
DQMM provides expertise in advanced quantitative
methods for the generic drug program and conducts GDUFA (Generic Drug User Fee
Amendments 2012) regulatory science and research activities based on
quantitative approaches, which include guidance development, abbreviated new
drug application (ANDA) reviews, citizen petitions, controlled correspondence,
pre-ANDA meetings, and methodology development for bioequivalence evaluation,
active ingredient sameness demonstration and post marketing safety
surveillance. This Division coordinates modeling, simulation, data
analysis and data mining and establishes the scientific computing
infrastructure for OGD. DQMM is also developing innovative quantitative
approaches to improve regulatory decision making for generic drugs by fully
utilizing the large amount of data available to FDA. The ORISE
position(s) at DQMM provides an outstanding opportunity to learn and apply
quantitative analysis, modeling, and simulation to support the aforementioned
activities.
Research at DQMM includes, but not limited to, the
following areas:
· Modeling and simulation of modified release solid oral
products (including absorption models, in vitro - in vivo correlations and
pharmacokinetic/pharmacodynamic [PK/PD] modeling) to ensure the consistency and
quality of bioequivalence recommendations from OGD.
· Model-based delivery system assessment.
· Innovative approaches to establish active ingredient
sameness/pharmaceutical equivalence for complex drug substances.
· In vitro bioequivalence analyses.
· Application of physiologically based pharmacokinetic
(PBPK) models for non-oral drug products to help develop new bioequivalence
methods for locally acting drug products administered via non-oral routes of
administration.
· PK/PD modeling of narrow therapeutic index drugs and
complex drug products and clinical trial simulation to aid risk-based
bioequivalence evaluation.
· Conventional and model-based meta-analysis on drugs
within same class or different classes.
· Conducting safety surveillance by developing/applying
novel analysis approaches to detect and assess safety signals of generic
products.
· Developing systems pharmacology-based methodologies to
understand and predict drug actions underlying both therapeutic effect and
adverse reactions.
· Establishing data infrastructure to increase ANDA
review efficiency and quality by providing integrated and readily searchable
information based on available NDAs and ANDA datasets regarding drug efficacy
and safety profiles.
Qualifications:
· Ph.D., M.D., Pharm.D., or other qualified scientists
holding advanced degree(s) in pharmacometrics, Clinical Pharmacology,
Pharmaceutical Sciences, Chemistry, Statistics, Life Science, or Engineering.
· Hands-on experience with modeling and simulation
software (e.g. NONMEM, SAS, Splus/R, Phoenix, Monolix, MATLAB, C++, GastroPlus,
Simcyp, PKSim, etc.).
· Good knowledge of formulation design,
biopharmaceutics, data analysis and/or modeling and simulation principles.
· Good scientific writing, communication, critical
thinking, and interpersonal skills.
For ORISE positions, the initial appointment is for
one year.
Location:
Silver Spring, MD
Contact:
Send CV to Jae Wook Yoo, Pharm D
[email protected]
Applications should be sent by 9/30/2016 to receive
full consideration.
Thanks,
Mario
Gonzalez Sales, Ph.D
Division
of Quantitative Methods and Modelling
ORS/OGD/CDER/FDA
10903
New Hampshire Ave., Bldg 75, Room 4695
Silver
Spring, MD 20993
Phone:
(301)-796-7365
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