At PRA, we don’t make our 15000+ people great. It’s the other way around. As we have grown to a top-5 CRO, we have maintained the feel of a small company, dedicated to collaboration and passion for what we do.
We always have a desire to keep seeking new and better ways to operate. We don’t settle for the same old ways. Our passion for improving patient lives worldwide permeates all that we do. Put simply, we care.
Working throughout the clinical drug development process through to final clinical study stage, the overall aim of this role is to ensure maintenance of stock of investigational products at sites across the world. In this role, you will ensure that appropriate processes are established and followed to achieve key clinical supplies deliverables, namely uninterrupted clinical supply is achieved throughout the duration of the clinical study.
Reporting to the Associate Director of Clinical Supplies and working on global studies, your key areas of responsibilities will include:
In this role, you will collaborate closely with other functional areas including clinical teams, regulatory, external vendors, CMC, in-licensing and QA partners
This role sits within one of PRA’s key client partnerships with a global pharma. The working environment in this group is innovative, credible and stimulating.
Analytical, forward-thinking and flexible.
Here at PRA we want our employees to succeed and ensure that they are set up for this success through constant training, development and support. To enable success in this position you will have:
Your health, your family, your career, your money — the things that matter to you, matter to us. The benefits of PRA just get better and better.
PRA Health Sciences is an Equal Opportunity Employer. We welcome and encourage diversity in the workplace.
For more information please visit our website: www.prahs.com