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0.0 - 4.0 years

0 Lacs

nashik, maharashtra

On-site

As a Clinical Research Associate, your responsibilities will include developing and reviewing study protocols and informed consent documents, monitoring clinical trial progress to ensure adherence to GCP, FDA, and IRB regulations, collecting, managing, and analyzing clinical data, preparing regulatory submissions and study reports, and collaborating with cross-functional teams including investigators and coordinators. This is a full-time position suitable for freshers. The benefits include health insurance. The work schedule is during the day shift and the work location is in person.,

Posted 2 weeks ago

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