Who are you - You are a highly skilled technical writer looking to join a growing world-wide organization. Looking to use and expand your skills to support our development and deployment of clinical trial management applications. In this position, you will create easy-to-understand user content and product documentation to increase product clarity, performance, and usability. Your strong knowledge base and ability to work cooperatively with other teams are a must. Most of all, you want to do it in a place where you’re more than an employee number. A place you love working.
What will you be doing – You will work collaboratively with designers and developers to provide comprehensive documentation for our suite of state-of-the-art clinical trial management applications. From administrator to end users, your content will be used to improve the user experience and guide administrators through the steps required to launch and maintain trials and studies from recruitment trough enrollment all the way to successful completion.
What you need to have:
PRA is an EEO/AA employer and is committed to providing opportunities to minorities, women, veterans and individuals with disabilities.