Clinical Trial Medical Monitor: Safety & Oversight

GE HealthCare; Paris; Presencial; EUR 85.000 - 110.000; Jornada completa

Descripción de la vacante

GE HealthCare is seeking a Medical Monitor to provide day‑to‑day medical oversight for clinical trials, ensuring patient safety, data integrity, and protocol compliance. The role collaborates with Clinical Operations, Pharmacovigilance, Data Management, Biostatistics, and Regulatory Affairs to support high‑quality clinical data and timely issue resolution.

The candidate should have an MD or equivalent and 3–7 years of experience in clinical trial execution, with strong GCP knowledge and

Formación

• 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.

Responsabilidades

• 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/SAEs and participate in safety reviews and DSMBs as required.
• Serve as a key medical contact for investigators and support site engagement with study‑specific input.
• Collaborate with cross‑functional teams to support safe and compliant study conduct.
• Contribute to regulatory submissions and maintain accurate study documentation.

Conocimientos

MD or equivalent

Clinical trial oversight

GCP knowledge

AE/SAE review

Descripción del empleo

GE HealthCare is seeking a Medical Monitor to provide day‑to‑day medical oversight for clinical trials, ensuring patient safety, data integrity, and protocol compliance. The role collaborates with Clinical Operations, Pharmacovigilance, Data Management, Biostatistics, and Regulatory Affairs to support high‑quality clinical data and timely issue resolution.

The candidate should have an MD or equivalent and 3–7 years of experience in clinical trial execution, with strong GCP knowledge and