Responsible for the safety and efficacy in the target species for new animal pharmaceutical research and development projects, line extensions and maintaining existing licensed products. Provides clinical study design and implementation including resource and budget planning from protocol to execution and to final study report for submission to regulatory agencies for animal pharmaceutical projects in both lab and field conditions. Fulfills a role as a subject matter expert in representing his/her function (e.g. on development teams, regulatory authority meetings and key Opinion Leaders). Acts as the Clinical Representative as assigned for all stages of product development. Presents clinical content to regulatory authorities as required and ensures compliance w
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