Vice President, Early Phase Development Center of Excellence, Scientific Strategy, IQVIA


Vice President, Early Phase Development Center of Excellence, Scientific Strategy, IQVIA
Vice President, Medical Strategy, Early Phase Development, IQVIA
Vice President, Therapeutic Strategy, IQVIA
In today’s rapidly evolving drug development landscape, early-phase clinical trials face mounting pressures: rising costs, shifting regulatory frameworks, geopolitical uncertainties, and heightened investor scrutiny. Yet, these challenges also open the door to transformative opportunities and “out of the box” thinking.
This webinar will explore how sponsors and CRO partners can leverage innovative trial methodologies — including customized adaptive designs, hybrid approaches, and model informed drug development (MIDD)— to generate high-quality data faster, make more informed go/no go decisions, and safely accelerate molecule progression.
Key discussion points will include:
Three key take-aways
For more information and to register, click here.