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5.0 - 9.0 years

0 Lacs

hyderabad, telangana

On-site

As a Medical Monitor, you will be responsible for overseeing the medical aspects of in-house clinical trials and managing the CRO's medical monitoring for outsourced projects. Your duties will include developing and reviewing various clinical documents such as protocols, investigator's brochures, case record forms, product rationales, prescribing information, and drug interactions. You will also be tasked with organizing materials for Subject Expert Committee (SEC) meetings and actively participating in these meetings to support clinical trials and marketing approvals. In addition to the primary responsibilities, you will be involved in the medical review of Individual Case Safety Reports (I...

Posted 1 month ago

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