New
Medical Monitor
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![]() United States, Illinois, Avon | |
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Job title: Medical Monitor
Location: Remote Duration: 12 Months Purpose: Describe the primary goals, objectives or functions or outputs of this position. Responsible for supporting the clinical development Neuroscience team with medical and safety monitoring. Responsibilities: List up to 10 main responsibilities for the job. Include information about the accountability and scope. * Provides medical monitoring and observation of clinical trials to ensure safety and adherence to protocol. * Coordinates, conducts, and communicates overview of safety data and significant changes to the study team. * Provide medical review, comment and assessment of causality for Serious Adverse Events (SAEs) * Responsible for medical monitoring of assigned studies including data reviews, queries assigned in TESLA * Participates in Product Safety Team meetings * Reviews CSRs/IBs/submissions, etc. * Peer review draft DRC materials * Monitor and compile competitive intelligence (landscape) assessments/white papers and provide medical perspective/implications * Assesses start-up requirements for EDC to ensure studies are set up properly for medical monitoring in collaboration with study team. * Conducts literature reviews at the request of study teams Qualifications: List required and preferred qualifications (up to 10). Include education, skills and experience. * MD/DO with 2+ years clinical development experience conducting medical monitoring for clinical trials. What are the top 3-5 skills, experience or education required for this position: 1. Medical Monitoring experience (later stage trials preferred) 2. Excellent communication and interpersonal skills 3. Ability to work independently |