Centre Hospitalier du Mans

About the Company

Situé au centre du territoire sarthois, établissement support du GHT 72, le Centre Hospitalier du Mans est l’établissement de référence, mais aussi l’un des plus grands hôpitaux non universitaires de France, y compris dans le domaine de la recherche clinique. Il offre des soins dans la totalité des spécialités médicales et chirurgicales (excepté la chirurgie cardiaque et la neurochirurgie). Le CH Le Mans est l’établissement siège du SAMU 72 et de son service mobile d’urgence et de réanimation (SMUR). Il dispose d’un plateau technique complet, avec notamment 23 salles d’opération, et propose également 300 places en EHPAD, principalement sur son site d’Allonnes. Il accueille en formation environ 200 internes et 60 externes, en permanence, et dispose d’un institut de formation en soins infirmiers (IFSI) et d’un institut de formation d’aides-soignants (IFAS). Le Centre Hospitalier du Mans est membre de la Direction commune des Hôpitaux de Sarthe avec les centre hospitaliers de La Ferté-Bernard, de Saint-Calais, de Montval-sur-Loir, du Lude et du Pôle Santé Sarthe et Loir.

Listed Jobs

Company Name

Centre Hospitalier du Mans

Job Title

Chef de projet ARC h/f - Recherche clinique

Job Description

**Job Title:** Clinical Research Project Manager **Role Summary:** Oversee end-to-end management of clinical research projects, ensuring administrative, logistical, regulatory, and scientific compliance. Coordinate stakeholders and maintain adherence to clinical standards. **Expectations:** - Contribute to protocol development and submission to tenders. - Ensure regulatory compliance of documents for EU/FR ethics boards. - Support data managers in designing observation tools and validating procedures. - Develop feasibility questionnaires, investigator files, and study-related documents. - Manage study logistics (material preparation, distribution). - Coordinate multi-site study implementation and adverse event monitoring. - Oversee data monitoring, audit processes, and regulatory deadlines for trial closure. - Align internal procedures with Clinical Good Practices (BPC). **Key Responsibilities:** - Supervise administrative, financial, and regulatory management of clinical trials. - Facilitate tender processes and project implementation across sites. - Maintain scientific/technical quality control of promoted research projects. - Organize cross-functional collaboration with investigators and teams. - Track adverse events and implement pharmacovigilance protocols. - Coordinate audits and cross-site evaluations for quality assurance. **Required Skills:** - Strong project management and stakeholder coordination. - Technical/regulatory writing for protocols and submissions. - Expertise in clinical trial monitoring, data validation, and process compliance. - Problem-solving, decision-making, and team leadership. - Fluency in medical terminology and hospital workflows. - Advanced proficiency in scientific English (written/spoken). **Required Education & Certifications:** - Master’s Degree in Clinical Research, Scientific, or Medical Engineering/Pharmacy. - Doctoral-level training or PhD in Clinical Research (preferred). - Demonstrated experience in clinical project management (minimum 1–2 years). - In-depth knowledge of EU/French clinical regulations and Clinical Good Practices (BPC). - Valid certification in clinical research methodologies (if applicable).

Le mans, France

On site

11-09-2025