Clinical Research Associate Statistical Insights

2.0 - 6.0 years

0 Lacs

pune, maharashtra

On-site

The job involves providing clinical study start-up expertise and assisting the Lead CRA in preparing IRB submissions, including reviewing site-specific informed consent and assent forms. You will be responsible for tracking IRB submissions, collecting, reviewing, and processing essential documents, as well as identifying any issues that the site needs to address. Communicating updates needed to essential documents to the site is also an essential part of the role. Additionally, you will lead or support the setup and maintenance of the Trial Master File (TMF) and assist or participate in planning and conducting Investigators Meetings as necessary. This is a full-time position that offers the benefit of working from home.,

Posted 1 day ago

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