Prestige Scientific has been chosen by an EU pharmaceutical company to identify their first Associate Director, Regulatory Affairs at act as their Regulatory Lead with the Office of Prescription Drug Promotion (OPDP) for the launch of their first US product. This position reports to the VP, Head of Regulatory Affairs US and will be located in Boston, MA.
As a member of the US Review Committee team, the Associate Director, Regulatory Affairs will be responsible for providing input and advice on the review of promotional materials.
This is a unique opportunity for someone to lead the ad/promo function on the launch of a first oncology product.
For additional information, contact Prestige Scientific in confidence.