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5.0 - 9.0 years

0 Lacs

hyderabad, telangana

On-site

As a Medical Monitor, your primary responsibilities will include: - Monitoring the in-house clinical trials and overseeing CRO medical monitoring of outsourced projects - Developing and reviewing clinical documents such as protocol, investigator's brochure, case record form, product rationale, prescribing information, drug interactions, etc. - Organizing Subject Expert Committee meeting materials and attending SEC meetings for clinical trials and marketing approvals Your secondary responsibilities will involve: - Reviewing Medical Review of ICSRs, Aggregate reports, Signal reports, and Risk Management plans - Reviewing clinical and non-clinical overviews and summaries of CTD - Reviewing medi...

Posted 6 days ago

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