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Clinical Research Associate Novartis

4.0 - 8.0 years

0 Lacs

maharashtra

On-site

You will be responsible for monitoring patient data and study-related information at clinical study sites to ensure adherence to research protocols, regulatory requirements, and good clinical practices. Your role will involve providing input into data validation plans and ensuring timely and accurate monitoring of patient data. You may also be required to monitor study sites and audit facility selection. Key Responsibilities: - Act as the frontline liaison between Novartis and sites to ensure successful collaboration, meeting Novartis" expectations on milestones and deliverables with a true ownership mindset - Manage assigned study sites, conduct phase I-IV protocols according to the Monitor...

Posted 2 months ago

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