Job Information
- Location:
Los Angeles, California, United States
- Company Name:
University of Southern California and AbbVie, Inc.
- Position Title:
Postdoctoral Fellowship Opportunities
- Setting:
College/University
Description
One-year postdoctoral fellowships are available now at the University
of Southern California School of Pharmacy and AbbVie, Inc. in the
following disciplines:
- Clinical Pharmacology
- Immunology
- Research Pharmacology
- Toxicology
Apply through the USC School of Pharmacy online application at:
https://provost.sma.usc.edu/prog/fellowship/
Clinical Pharmacology Fellowship
This
non-laboratory based one-year Clinical Pharmacology Fellowship focuses
on developing skills of a modern clinical pharmacology scientist. The
fellow will be provided opportunities to gain expertise in nonclinical
and clinical development through honing skills in areas such as
nonclinical pharmacokinetics/toxicokinetics, clinical pharmacology,
translational strategies, modeling and simulation/pharmacometrics. As
part of the training, the fellow will be provided with opportunities to
engage in various activities such as: design and execution of
nonclinical pharmacokinetic/toxicokinetic studies, design and execution
of clinical pharmacology studies, development of translational
strategies in support of target engagement and biomarker/ dose/regimen
selection, preparation of regulatory documents, and PK/PD and pop-PK
modeling. The candidate will also participate in cross-functional team
interactions spanning all of AbbVie’s therapeutic areas. This advanced
hands-on training program can be tailored towards the specific needs and
background of the candidate.
Objectives:
- Collaboratively design and
oversee execution of nonclinical pharmacokinetic/toxicokinetic studies
and/or clinical pharmacology studies
- Analyze, interpret, and present data derived from nonclinical and clinical studies
- Serve
(alongside a senior mentor) as a representative on nonclinical and
clinical project teams to guide clinical pharmacology and translational
efforts
- Contribute towards drafting regulatory documents
- Execute, interpret, and present results from PK/PD and/or pop-PK analyses at internal meetings
- If applicable, present work at professional meetings and/or author a scientific publication
Please visit our Clinical Pharmacology Fellowship webpage for information at: https://pharmacyschool.usc.edu/programs/fellowship/clinical-pharmacology-fellowship/
Immunology Fellowship
The
one-year Immunology Fellowship mainly focuses on immunogenicity studies
against biologics and toxins to support drug development programs. As
part of the training, the fellow will be provided with opportunities to
participate in various activities like designing experiments, executing
experiments and data analysis. It also involves cross functional team
interactions across multiple therapeutic areas within AbbVie.
Additionally, interested fellows can gain expertise in flowcytometry,
Luminex, ex vivo/in vivo assays. The fellowship is intended to enhance
the postdoctoral research training of the applicant and develop the
skills required to excel in their field.
Objectives:
- Collaborate
and conduct a thorough review and build a knowledge base
(ARCH/Convergence collaboration) of the immunogenicity data across all
internal ophthalmology, Toxin and device programs
- Build
knowledge base (collect, analyze data) for immunogenicity data and
potential risks from publications on commercial biologics across all
ophthalmology, Toxin and device areas.
- Building knowledge base
from literatures around in silico and in vitro assays and identify the
most promising ones for immunogenicity prediction specific for different
modalities
- Proposing fit-for-purpose in vitro/ex vivo/in vivo
assays to investigate potential risk evaluation and relevant outcome
measures for devices
Please visit our Immunology Fellowship webpage for more information at: https://pharmacyschool.usc.edu/programs/fellowship/immunology-fellowship/
Research Pharmacology Fellowship
This
one-year Research Pharmacology Fellowship focuses on developing the
pre-clinical translational skills required of a pharmacology scientist.
As part of the training program, the fellow will participate in
pre-clinical study activities including study conceptualization through
study design, protocol development, study execution, and cross
functional team interactions across multiple therapeutic areas within
AbbVie. Additionally, interested fellows can gain expertise in
pharmacology sections of regulatory submissions, and interact with
scientists from other functions such as formulation development,
clinical pharmacology and clinical development. The fellowship is
intended to enhance the postdoctoral research training of the applicant
with hands-on application of core biological principles and techniques
to move programs from preclinical stages to clinical development for key
AbbVie programs.
Objectives:
- Independently design and conduct pharmacology studies to support program projects
- Research, design and validate novel platforms or targets
- Be able to execute, interpret, and deliver data analyses
- If applicable, present work at internal AbbVie meetings, a professional meeting and/or author a scientific publication
Please visit our Research Pharmacology Fellowship webpage for more information at: https://pharmacyschool.usc.edu/programs/fellowship/research-pharmacology-fellowship/
Toxicology Fellowship
The
one-year Toxicology Fellowship focuses on developing the skills needed
to identify the toxicology and safety pharmacology studies required to
support drug development programs, to independently design toxicology
studies and to be able to interpret and integrate data from toxicology
studies into risk assessments in support of product safety and dose
selection for initiating clinical investigations or regulatory
submissions. As part of the training, the fellow will engage as
Toxicology Representative on project teams, prepare regulatory
documents, learn about the assessment of testing facilities and
participate in cross-functional team interactions.
Objectives:
- Learn
about requirements for nonclinical safety testing of pharmaceutical
drugs to support conduct of clinical trials and marketing authorization
- Learn how to independently design and conduct toxicology studies
- Acquire experience as Toxicology Representative on projects teams to guide the nonclinical safety strategy
- Be able to interpret data from toxicology studies
- Become familiar with global regulatory agency interactions and regulatory document submissions
- Participate in/observe nonclinical safety study activities
Please visit our Toxicology Fellowship webpage for more information at: https://pharmacyschool.usc.edu/programs/fellowship/toxicology-fellowship/
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