Fellowship Opportunities
Research Fellowship: Pediatric Movement Disorders
Qualifications:
Applicants must have completed training in an accredited Pediatric, Neurology, or Child Neurology training program.
Duration:
1 – 2 years
Salary:
PGY IV level
Job Description:
The goal of this fellowship opportunity is to provide a multi-disciplinary research experience with a specific focus on Alternating Hemiplegia of Childhood. Fellows will have the opportunity for a broad clinical exposure to pediatric motor disorders, with specific emphasis on diagnostic approaches, clinical management and treatment. The primary goal of this program is to provide a mentored research experience designed to enhance our understanding of clinical and basic science approaches which will lead to improvements in the diagnosis and treatment of AHC patients. The fellow will serve primarily in a research capacity, but depending on his/her qualifications, may be involved in clinical care when included as part of a research protocol. Responsibilities will include:
- Database management and analysis, with emphasis on producing manuscripts for peer-reviewed publication. We have established a patient registry for children affected with AHC, with associated clinical and molecular databases which serve as a valuable starting point to answer specific research questions. The fellow will work closely with a clinical research coordinator to help maintain and expand the database.
- Continued genetic research, specifically in regard to AHC, through the use of Gene Chip or Microarray analysis. As yet, no genetic basis has been established for AHC, despite considerable efforts. As technology continues to evolve, the fellow will assist the PI with investigation into possible genetic etiologies for AHC, both at the Utah site, and in collaboration with other laboratories nationally and internationally.
- Development and execution of clinical trials for potential therapies for children with AHC. The fellow will help to formulate experimental protocols, as well as manage regulatory documentation required in the development of new therapies.
- Grant preparation and submission is a necessary component in the study of these rare disorders. As a result, the fellow will assist the PI in preparation and submission of grant materials related to current and future areas of interest.
- Patient and family support is critical in providing comprehensive care to children and families affected by neurodegenerative disorders. In conjunction with the AHC Foundation, the fellow will serve as resource as families attempt to better understand their child’s disease, as well as the current state of research.
- Tissue and DNA biobank for ongoing development of a repository of DNA, RNA, cell lines and tissue resources to help facilitate a better understanding of the pathophysiology of this complex disease. This resource will be available to any investigators interested in collaborating in research on AHC.
Expectations:
Production of at least two to three manuscripts appropriate for peer-reviewed publication, working closely in conjunction with Dr. Swoboda, the principal investigator.
How to Apply:
Please send a letter of intent and copy of your CV to:
Dr. Sandy Reyna
sreyna@genetics.utah.edu
You may call the Pediatric Motor Disorders Research Program at 801.585.9717 for more information.