Clinical Research Associate Refined Reports Data

0.0 - 4.0 years

0 Lacs

ahmedabad, gujarat

On-site

As a Clinical Research Associate, your role involves creating and writing trial protocols, presenting them to the steering committee, and identifying trial sites. You will also be responsible for training site staff on therapeutic areas, protocol requirements, and proper documentation. Furthermore, you will liaise with the ethics committee to ensure the rights and safety of trial subjects. Key Responsibilities: - Creating and writing trial protocols - Identifying and establishing trial sites - Training site staff on therapeutic areas and protocol requirements - Liaising with the ethics committee - Ordering, tracking, and managing IP and trial materials - Overseeing IP dispensing inventory an...

Posted 1 day ago

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