Medical Monitor - CNS

Cognitive Research Corporation • Remote, US • published 2026-09-23 05:43:16.114366

Description

The Medical Monitor (MM) plays a critical role in overseeing the safety and efficacy of clinical trials, ensuring compliance with regulatory requirements, providing medical oversight, and performing medical data reviews to ensure patient safety and data integrity. Collaborates with Project Manager, Safety/Pharmacovigilance (PvG), Data Management, Biostatistics, QA, Principal Investigator and Sub\-investigators, Site Coordinators, the Data Monitoring Committee (DMC), and any other group that directly or indirectly protects the safety of study participants. **Essential Duties and Responsibilities:** **Clinical Trial Medical Oversight:** Provide medical, scientific, and safety oversight for clinical trials, ensuring protocol adherence, participant safety, eligibility, IP dosing, and management of AEs/SAEs/SUSARs, with 24/7 coverage and backup support as needed. **Safety Review \& Risk Management:** Lead and support ongoing safety data review, including medical coding, patient narratives, Risk Management Plans, MedWatch reporting, and collaboration with Safety/PvG, DMCs, and cross‑functional teams. **Site \& Investigator Support:** Serve as the primary medical point of contact for inve...

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