Job Description

This is an engaging and responsible role within an international environment. Working as a part of PAREXEL Consulting Services, you will prepare and submit clinical trial applications to regulatory authorities, whilst providing regulatory consultancy and strategy to project teams and responding to ad hoc requests for licensing of medicinal products.

Requirements

-

Company offers

In return, we offer a competitive salary and benefit package, opportunities for career development and personal growth, and a stable team - all in a highly professional working environment within one of the leading CROs.

Additional information

To apply, please send your CV (preferred as a word document) and covering letter, stating the role for which you wish to apply, to HR-Europe@parexel.com