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1.0 - 4.0 years
12 - 18 Lacs
gandhinagar, ahmedabad
Work from Office
Job Summary The Medical Monitor will serve as the primary medical expert for late-phase (Phase IIIV) clinical trials, ensuring subject safety, scientific integrity, and regulatory compliance throughout the study. This role involves providing ongoing medical oversight, safety data review, protocol compliance assessment, and guidance to investigators and the clinical team. The Medical Monitor acts as the key medical contact for study teams, sites, sponsors, and regulatory authorities. Key Responsibilities Provide continuous medical and scientific oversight for late-phase clinical studies. Ensure subject safety through regular review of adverse events, SAEs, and safety signals. Conduct medical ...
Posted 1 week ago
2.0 - 5.0 years
10 - 20 Lacs
hyderabad
Work from Office
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 1 month ago
1.0 - 4.0 years
12 - 18 Lacs
gandhinagar, ahmedabad
Work from Office
Job Summary The Medical Monitor will serve as the primary medical expert for late-phase (Phase IIIV) clinical trials, ensuring subject safety, scientific integrity, and regulatory compliance throughout the study. This role involves providing ongoing medical oversight, safety data review, protocol compliance assessment, and guidance to investigators and the clinical team. The Medical Monitor acts as the key medical contact for study teams, sites, sponsors, and regulatory authorities. Key Responsibilities Provide continuous medical and scientific oversight for late-phase clinical studies. Ensure subject safety through regular review of adverse events, SAEs, and safety signals. Conduct medical ...
Posted 1 month ago
4 - 9 years
7 - 10 Lacs
Mumbai, Hyderabad, Pune
Work from Office
• MBBS/ MD with clinical exp • Review protocol and provide suggestions • Respond to queries/ clarifications from EC/ IRBs • Answer medical questions from sites or project team • Respond to queries from sites with regard to protocol
Posted 6 months ago
8 - 12 years
12 - 22 Lacs
Pune, Bengaluru, Mumbai (All Areas)
Work from Office
Hi We are looking forward to hire Medical Monitor for our Client. Please go through the JD and Apply Responsibilities: Review protocol and provide suggestions Respond to queries/ clarifications from EC/ IRBs Answer medical questions from sites or project team Respond to queries from sites with regard to protocol Attend drug safety meetings/ external meetings Patient eligibility review Review AE/ SAEs Protocol training to site staff, CRAs etc Attend, participate/ present in investigator meetings Qualification: MBBS/ MD qualification Eligibility: 3 year+ of clinical trial experience Familiar with clinical trials operations Good English communication skills Proficiency in using Microsoft office...
Posted 6 months ago
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