**More about you**On your first day we'll expect you to have:- Site Management or equivalent experience in clinical research, with understanding of clinical trials methodology and terminology.- Ability to perform all clinical monitoring activities independently.- Bachelor's or equivalent degree in biological science, pharmacy or other health related discipline.- Strong interpersonal, written, and verbal communication skills within a matrixed team.- Experience working in a self-driven capacity, with a sense of urgency and limited oversight.- A client-focused approach to work and flexible attitude with respect to assignments/new learning.- An honest and ethical work approach to promote the development of life changing treatments for patients.- Strong computer skills, including but not limited to the knowledge of a Clinical Trial Management System (CTMS), Electronic Document Management System (EDMS) and MS-Office products such as Excel and Word.**A little about us**Parexel is proud to be a leading Clinical Research Organization with colleagues across the globe. As a member of our team, you'll get to know your coworkers on a personal level. Have a question? A clinical research leader, project team member, technology "super user" or collaborator are a phone call away. Our clinical research teams meet regularly to have discussions in an open environment, allowing our team members to share their expertise and promote learning within the team. Management supports and encourages career growth through consistent performance discussions and evaluations. Whether your interest is to progress into a more senior level CRA role, into line management, Quality, Project Leadership or a variety of other positions, Parexel prides itself on career opportunities for our employees.