Clinical Research Coordinator
Posted 24 days ago
- Leeds, West Yorkshire
- Any
- External
- Expires In 2 months
This is an exciting opportunity with candidates to start and interview as soon as possible!
The Study Coordinator must have minimum 1 year clinical research experience as they need an individual who can work independently as well as part of a team. Day to day responsibilities will involve a reporting adverse events, data entry, administrative tasks and query resolution.
The Study Coordinator must have minimum 1 year clinical research experience as they need an individual who can work independently as well as part of a team. Day to day responsibilities will involve a reporting adverse events, data entry, administrative tasks and query resolution.
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