Description
Roles and Responsibilities:- Provide logistical support for Study Team
- Develop, maintain and manage appropriate study documentation
- Collect, review and approve regulatory documents from clinical sites
- Initiate, maintain and reconcile Trial Master File
- Set up and maintain tracking systems and tools and report study metrics to support the clinical study
- Manage and track clinical and non-clinical supplies
Requirements:
- 2+ years of industry experience in equivalent role
- Bachelor's degree or equivalent undergraduate degree required
- Working knowledge of international regulatory and ICH GCP guidelines
- Proven organizational skills demonstrated by the ability to understand and prioritize instructions and deliver on time
To find out more about Real please visit www.realstaffing.com