Clinical Medical Monitor
Core
Provide hands-on medical oversight for clinical programs, ensuring patient safety and study quality by supporting investigators and sites with medical guidance, safety assessments, and data surveillance.
Role type
Senior IC Clinical Medical Monitor (Director/Senior Director level)
Builds
Clinical development programs for CNS disorders
Domain
Biopharmaceuticals / Clinical Development / Central Nervous System
Deliverable
production ML models | product features | dashboards & analysis | research | client delivery | infrastructure | physical/clinical work
Required skills
Medical judgment, Clinical safety assessment, GCP knowledge, Data surveillance, Cross-functional partnership, Independent decision-making
Preferred skills
CNS therapeutic area experience, Director/Senior Director level experience
Technologies
Clinical trial safety reporting systems, Data management tools
Responsibilities
Provide timely medical guidance on eligibility, dosing, and protocol requirements; Review and assess adverse events (AEs) and serious adverse events (SAEs) for causality and clinical significance; Respond to investigator and site medical questions; Monitor clinical and safety data to identify emerging signals; Ensure compliance with regulatory requirements and study protocols; Partner with cross-functional teams to resolve issues.
Seniority
Senior, hands-on IC (Director or Senior Director level)