How your CV stacks up
Upload your CV to see how well it fits this job role
?%
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
GE HealthCare is a leading global medical technology and digital solutions innovator. Our purpose is to create a world where healthcare has no limits. Unlock your ambition, turn ideas into world-changing realities, and join an organization where every voice makes a difference, and every difference builds a healthier world.
Key Responsibilities
Clinical Trial Medical Oversight
- 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.
Reasons to use Rodeo
Start with a chat, not a search bar
Grad scheme, placement, apprenticeship? Not sure what you want yet — that's fine. Your agent talks it through with you and turns "I have no idea" into a shortlist.
It searches the market for you
Every day your agent scans the market matching roles against what actually matters to you, not just keywords on a CV.
Only hits
No noise. No "maybe this fits." Just roles with a clear explanation of why they're right — and where to focus when applying.
Safety Monitoring & Signal Detection
- Review and assess AEs and SAEs, including causality and severity evaluations.
- Participate in ongoing safety reviews, internal safety committees, and Data Safety Monitoring Boards (DSMBs) as required.
- Collaborate closely with Pharmacovigilance to support safety signal detection, escalation, and risk-management actions.
- Support development and implementation of protocol amendments or safety measures when indicated.
Site & Investigator Support
- Serve as a key medical contact for investigators, responding to protocol-specific medical questions and eligibility clarifications.
- Support investigator meetings and site engagement activities with study-specific medical input.
- Provide medical oversight and guidance when studies are conducted with CRO medical monitors, ensuring consistency with GE HealthCare expectations.
Cross-Functional Study Team Collaboration
- Work closely with Clinical Trial Leads (CTLs), Clinical Project Managers (CPMs), CRAs, Data Management, and Biostatistics to support smooth trial execution.
- Participate in operational safety and study management meetings, contributing medical perspective to study-level decisions.
- Support timely identification and resolution of safety or operational risks impacting study conduct.
Regulatory & Documentation Support
- Contribute to clinical study reports (CSRs), safety narratives, and regulatory submission documents.
- Ensure accuracy and consistency of medical data in study documentation and regulatory deliverables.
- Support regulatory interactions by addressing detailed clinical execution and safety questions as required.
- Ensure appropriate SAE reconciliation and alignment between clinical, safety, and regulatory datasets.
Get help with your application
Your very own career expert that helps elevate your application to the next level.
Required Qualifications
- 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.
Desired Characteristics
- 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.
Additional Information
- Relocation Assistance Provided: No
- Application Deadline: julio 29, 2026
At GE HealthCare, we see possibilities through innovation. We’re partnering with our customers to fulfill healthcare’s greatest potential through groundbreaking medical technology, intelligent devices, and care solutions. Better tools enabling better patient care. Together, we are not only building a healthier future but living our purpose to create a world where healthcare has no limits.
“It took my CV and asked me questions relevant to understanding what kind of jobs to suggest for me. Suggestions were almost perfect. Jobs were exactly what I’ve been looking for.”
Jessica, London
Skills
Location