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MIDD approaches can advance the understanding of pharmacological activity, efficacy and safety Provide support in the development and application of state-of-the-art quantitative methodologies
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for regulatory submissions. Knowledge of experimental design. Strong understanding of the state-of-the-art technologies to evaluate and leverage them for improved business processes. Aptitude to identify
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-on expertise in state of the art genetic and epigenetic approaches coupled with next-generation sequencing technologies to gain a broader understanding of MOA and target validation of novel cancer therapeutics
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