Medical Monitor

🕒 5 days ago

🇬🇧 United Kingdom – Remote

⏰ Full Time

🟡 Mid-level

🟠 Senior

🧪 Clinical Research

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GE HealthCare

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10,000+ employees

Founded 1892

🏥 Healthcare

💊 Pharmaceuticals

Healthcare • Medical Technology • Pharmaceuticals

GE HealthCare is a leader in precision care, dedicated to providing innovative technologies and integrated solutions that enhance healthcare services. As a stand-alone company, it focuses on imaging, ultrasound, and healthcare IT, empowering clinicians and improving patient outcomes through advanced medical technologies and personalized care solutions. With a significant investment in research and development, GE HealthCare aims to transform healthcare by making hospitals more efficient and therapies more precise.

📋 Description

• Provide medical oversight for one or more assigned clinical trials within a program or portfolio • Ensure patient safety and protocol-compliant execution throughout trial conduct • Apply medical judgment to eligibility questions, protocol deviations, dosing decisions, and participant risk mitigation • Review and assess AEs and SAEs, including causality and severity evaluations • Participate in ongoing safety reviews, internal safety committees, and Data Safety Monitoring Boards as required • Collaborate with Pharmacovigilance on safety signal detection, escalation, and risk-management actions • Support protocol amendments or safety measures when indicated • Serve as a key medical contact for investigators and answer protocol-specific medical questions • Support investigator meetings and site engagement activities with study-specific medical input • Provide oversight when studies are conducted with CRO medical monitors • Collaborate with Clinical Trial Leads, Clinical Project Managers, CRAs, Data Management, and Biostatistics • Participate in operational safety and study management meetings • Identify and resolve safety or operational risks affecting study conduct • Contribute to clinical study reports, safety narratives, and regulatory submission documents • Ensure accuracy and consistency of medical data in study documentation and regulatory deliverables • Support regulatory interactions by addressing clinical execution and safety questions • Ensure SAE reconciliation and alignment between clinical, safety, and regulatory datasets

🎯 Requirements

• MD or equivalent medical degree • 3–7 years of experience in clinical trial execution, medical monitoring, or related roles • Strong knowledge of GCP, clinical trial conduct, and safety reporting requirements • Experience reviewing AEs/SAEs and participating in safety oversight activities • Ability to work within protocol and regulatory frameworks while applying sound medical judgment • Strong clinical judgment with attention to patient safety and data quality • Solid understanding of clinical trial methodology and operational execution • Ability to collaborate effectively within cross-functional and matrixed teams • Clear and professional communication with investigators and study stakeholders • Detail-oriented, with strong documentation and compliance mindset

🏖️ Benefits

• Relocation assistance not provided

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