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Genome wide association studies (GWAS) have identified numerous common genetic variants associated with the risk of CHD as well as platelet functional parameters. However, most of these GWAS “hits” are in introns or inter-genic sequence, such that the responsible genes and variants are unknown. A postdoctoral position is available for candidates to contribute to the identification of genetic variants that alter platelet function and associate with thrombotic diseases. The candidate must have experience with cell culture, molecular and cellular biology, and flow cytometry. A background in genetics, hematology, or gene expression would be viewed favorably. This position provides an excellent opportunity to grow scientifically and work with a dynamic group of investigators studying important and exciting aspects of vascular thrombosis. Some experience with bioinformatics is desired.

Applicant should have a PhD in biology, molecular biology, cell biology, physiology, biochemistry, vascular biology, or a relevant discipline. A background in genetics, gene expression, epigenetics and/or computational analysis of large data sets would be viewed favorably..

• Ph.D. required
• Handling human blood and platelets
• An understanding of biochemistry and molecular biology
• Ability to learn new biochemical and physiological techniques
• Ability to work independently
• Ability to present work at national meetings, prepare manuscripts for submission
• Minimum 2 to 3 year commitment
• Familiarity with various computer programs such as word, excel, powerpoint, and prism.
• Interacts with co-workers, visitors, and other staff consistent with the core values of the University….