**Job Description Summary**
The Medical Monitor, Clinical Development is responsible for providing day‑to‑day medical oversight for one or more clinical trials to ensure patient safety, data integrity, and protocol compliance throughout trial execution. This role serves as the primary medical point of contact for study teams and clinical sites, supporting safe and compliant study conduct in alignment with Good Clinical Practice (GCP) and regulatory requirements.

Operating within defined protocols and development strategies, the Medical Monitor provides medical judgment during trial execution, including safety signal evaluation, eligibility assessments, dose modifications, and risk mitigation. The role works closely with Clinical Operations, Pharmacovigilance, Data Management, Biostatistics, and Regulatory Affairs to support operational excellence, timely issue resolution, and high‑quality clinical data.

GE HealthCare is a leading global medical technology and digit...