CHR Metz-Thionville

About the Company

Le CHR Metz-Thionville est un établissement bi-site distant de 30 km, Metz et Thionville, comprenant au total 8 établissements.
Hôpital de Mercy (Metz), hôpital Bel-Air (Thionville), hôpital Femme Mère Enfant, hôpital d'Hayange (Hayange), hôpital Félix Maréchal (Metz) et deux maisons de retraite à Metz (Saint-Jean et Le Parc).

Avec près de 2085 lits plus de 5500 agents, le CHR Metz-Thionville est reconnu comme le plus important sur son territoire de santé (600 000 personnes) couvrant un champ d'activités complet. Il est également une structure de recours qui répond au mieux aux besoins de la population: pôle mère-enfant, psychiatrie et pédo-psychiatrie, spécialités médicales, chirurgie, service des urgences, service des brûlés , soins palliatifs, gériatrie.

Listed Jobs

Company Name

CHR Metz-Thionville

Job Title

Attaché de recherche clinique Monitoring H-F

Job Description

**Job Title** Clinical Monitoring Attaché (H/F) **Role Summary** The Clinical Monitoring Attaché supports the internal promotional research programme of a multi‑site hospital group. The role ensures data quality, regulatory compliance, and efficient operation of clinical studies across all sites, and participates in study planning, documentation, and logistical coordination. **Expectations** - Work full‑time (100%) under the internal promotion manager. - Travel nationally and regionally to study sites, including off‑site investigator centres. - Maintain rigour, organisational skills, and strong written and verbal communication, especially in scientific English. **Key Responsibilities** - Monitor and verify data quality for internal studies across all hospital sites. - Ensure regulatory compliance of study documents and observe alignment between clinical data and patient medical records. - Confirm proper reporting of adverse events to the sponsor. - Review study protocols and assist in generating study deliverables: observation notebooks, data entry guides, monitoring plans, and manuals. - Manage logistics of trial initiation and closure visits, collaborating with project leads. - Track and record additional information requests (EIGs), coordinating with pharmacovigilance and material safety teams. - Support continuous site monitoring and provide quality‑related documentation updates. **Required Skills** - Scientific rigour and meticulous attention to detail. - Strong organisational and project‑management abilities. - Excellent written and verbal communication, including scientific English comprehension. - Proficiency with Microsoft Office Suite (Word, Excel, PowerPoint), email, and web research. - Interpersonal skills for effective collaboration with investigators, coordinators, statisticians, and regulatory bodies. - Flexibility and willingness to travel beyond the primary hospital group. **Required Education & Certifications** - Minimum Bac +5 in life sciences, medicine, or related field. - Clinical research training and/or experience (e.g., DIU FARC, FIEC, or equivalent). - Knowledge of current clinical research regulations and guidelines.

Metz, France

Hybrid

17-11-2025