The representative, In collaboration with various operational counterparts within the company and with external suppliers/vendors, Will ensure therapeutic strategy development and the clinical and operational execution of company sponsored studies, detective initiated studies and post marketing risk management research programs, in the course of in sourced, Outsourced or matrixed others. those will focus on Phase II Phase IV studies, Post marketing risk management research programs and IIS trials to ensure strategic level plans are executed in a timely and compliant fashion for victory of Medical Affairs' research goals. Manage and be accountable for budgets for multiple therapeutic areas across the portfolio.

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