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2.0 - 5.0 years

10 - 20 Lacs

hyderabad

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Role & responsibilities Provide comprehensive medical and scientific expertise and oversight for clinical trials, ensuring study integrity and participant safety. Review and contribute medical input to study protocols, ensuring clinical feasibility, scientific rigor, and compliance with regulatory requirements and guidelines. Ensure strict adherence to clinical trial protocols through continuous monitoring and proactive management of ongoing studies. Prepare, critically review, and approve essential clinical trial documents across all phases, including Informed Consent Forms (ICF), Statistical Analysis Plans (SAP), Clinical Study Reports (CSR), Safety Management Plans, Medical Management Pla...

Posted 11 hours ago

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