Regulatory Affairs Associate (Global RA Manager-AdPromo)

We are currently recruiting for a number of Regulatory Affairs Associates in Romania to be dedicated to client-dedicated projects.

A Regulatory Affairs Associate must have an understanding of the organization’s consulting models and methodologies, as well as, good knowledge of what services Parexel Consulting provides. A Regulatory Affairs Associate must have good technical skills and may be developing specialist knowledge of a particular subject and/ or market. A Regulatory Affairs Associate ensures the timely performance of work within a project scope to the quality expectations of PC and the client.

We are currently looking for a Regulatory Affairs Associate who will have the following responsibilities:

Key Responsibilities: Review, approval, and release of all advertising and promotional materials (promotional, disease awareness, institutional, training, and risk minimization tools) for products Review, approval, and release of all international congresses materials for products Writing and update of all controlled documents related to QMS supporting advertising and promotion (i.e. SOP, STD) QualificationsMedical doctor or advanced degree 2- 3 years of relevant experience at the global level Thorough understanding of specific regulatory requirements Strong problem solving and diplomacy skills Excellent project management skills Fluent English