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Qualifications:
Ph.D. and/or M.D. plus at least two years post-doctoral experience required. Experience must include application of Molecular Profiling technologies, analysis and interpretation of large microarray or gene expression data sets. Direct experience with clinical development, toxicogenomics, RNA therapeutics and strong statistical skills preferred. Excellent communication, collaboration, and organizational skills are essential.

Responsibilities:
This position, which will be based at West Point, PA, will have the following primary responsibilities: 1) collaborate with basic research, pre-clinical, and clinical scientists to design studies that heavily leverage MP technologies, with a primary emphasis on RNA profiling but also including genotyping, deep sequencing, proteomics and metabolomics 2) integrate data from internal experiments with data in the public domain for biomarker and target discovery 3) translate the results from MP studies to concrete deliverables that enable the drug discovery and development pipeline, and collaborate with statisticians and bench scientists to develop robust clinical biomarker assays 4) contribute biomarker sections to clinical development plans and clinical protocols 5) leverage MP technologies to provide novel readouts that can help maximize the development of RNA therapeutics and drug toxicity components 6) present analysis results.

• Location: West Point, PA
• Compensation: Based on experience
• This is a contract job.
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