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1.0 - 5.0 years

0 Lacs

ahmedabad, gujarat

On-site

As a Clinical Trial Coordinator, you will be responsible for overseeing the daily activities of clinical trials at various study sites. Your duties will include coordinating patient recruitment, screening, and assisting with the informed consent processes. Additionally, you will be tasked with maintaining trial documentation such as case report forms and regulatory binders. You will play a crucial role in scheduling and tracking study visits, as well as monitoring data collection and entry to ensure accuracy and compliance with protocols. Effective communication with investigators, sponsors, and ethics committees will be essential to the success of the trials. This is a full-time position that offers health insurance benefits. The working hours are during the day shift, and the job requires you to be present in person at the designated work location.,

Posted 2 weeks ago

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