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Clinical Research Associate (Fresher) Clariwell Global Services

0.0 - 4.0 years

0 Lacs

pune, maharashtra

On-site

You will be responsible for creating and writing trial protocols and presenting them to the steering committee. You will identify, evaluate, and establish trial sites, as well as close them down upon completion of the trial. Training site staff on therapeutic areas, protocol requirements, proper source documentation, and case report form completion will also be a key part of your role. Your duties will include liaising with the ethics committee to ensure the rights, safety, and well-being of trial subjects. You will be in charge of ordering, tracking, and managing investigational product (IP) and trial materials. Additionally, you will oversee and document IP dispensing inventory and reconci...

Posted 2 months ago

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