Regulatory Affairs Consultant - São Paulo, Brasil - Parexel

Descrição

Skills and knowledge:
Regulatory Affairs Consultant should have solid local expertise in submitting Clinical Trials to Health Authority in Brazil.

This role will be responsible for managing and coordinating the regulatory submission strategy for a large number of clinical trials in Brazil.

Also, will coordinate and manage flow of information, track project progress, and identify and solve problems in a team-oriented environment.

Good communication and leadership skills as well as team player attitude is needed to be successful in this position. Detail orientation and flexibility will be highly appreciated as well.