Description
Roles and Responsibilities:- Provide logistical support for Study Team
- Collect, review and approve regulatory documents from clinical sites
- Initiate, maintain and reconcile Trial Master File
- Coordinate communication of tracking information within Study Team and to sites
- Manager and track study specific payments
- Manage and track clinical and non-clinical supplies
- Develop study related documents in collaboration with the Study Team
Required Experience and Skills:
- 2+ years of industry experience in a equivalent role
- Bachelors degree or equivalent undergraduate degree (scientific or healthcare preferred)
- Working knowledge of international regulatory and ICH GCP guidelines
- Proven organizational skills demonstrated by the ability to understand and prioritize and deliver on time
- Experience using computer apps (email, word-processing software, web-based systems)
To find out more about Real please visit www.realstaffing.com