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CHRU de Strasbourg - Hôpitaux Universitaires de Strasbourg

CHRU de Strasbourg - Hôpitaux Universitaires de Strasbourg

www.chru-strasbourg.fr

3 Jobs

2,975 Employees

About the Company

Centre hospitalier universitaire. L'innovation en santé pour tous !

Listed Jobs

Company background Company brand
Company Name
CHRU de Strasbourg - Hôpitaux Universitaires de Strasbourg
Job Title
Ingénieur biostatisticien (H/F) - 100% - Spécialiste de l’utilisation secondaire des données de santé - Service de Santé publique
Job Description
**Job Title**: Biostatistician - Specialist in Secondary Use of Health Data - Public Health Service **Role Summary**: Lead statistical analysis of health data for a population stratification project to improve healthcare pathways. Focus on comparing predictive models for heart failure and diabetes type 2 using high-dimensional statistical methods and secondary health data from SNDS (French National Health Data System). **Expectations**: - Collaborate with medical and technical teams across research, IT, and clinical innovation departments. - Support project documentation and protocol development for SNDS data access. - Deliver analytical results for internal communication and scientific publication. **Key Responsibilities**: - Master two population stratification models (Fédération Hospitalière de France and IDIBAPS) for risk prediction. - Clean, cross-reference, and structure SNDS databases to identify patient cohorts for retrospective/Prospective Cohorts. - Design and execute high-dimension statistical analyses (e.g., machine learning, prediction modeling). - Develop analytical plans aligned with project goals (e.g., evaluating healthcare pathway effectiveness). **Required Skills**: - Expertise in statistical analysis of health data, including machine learning and R/Python. - Proficiency in working with national health databases (e.g., SNDS, CNAM). - Experience in cross-functional research teams with medical, public health, and IT professionals. - Ability to communicate findings to stakeholders through reports and publications. **Required Education & Certifications**: - Master’s or engineering degree in biostatistics, public health, or related field. - Prior experience in health research environments (hospital, academic, or government). - SNDS data handling certification preferred; if not certified, completion required upon hiring.
Strasbourg, France
On site
07-11-2025
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Company Name
CHRU de Strasbourg - Hôpitaux Universitaires de Strasbourg
Job Title
Technicien d’étude clinique (H/F) – 100% – Base de données et registres Maladie de l’oeil
Job Description
**Job title** Clinical Study Technician – Eye Disease Database & Registry (Full‑time) **Role Summary** Support the collection, entry, and management of clinical data for rare eye diseases in national and European registries. Contribute to data quality improvement, workflow optimisation, and the integration of automation or AI tools within the registry infrastructure. **Expectations** - Deliver accurate, timely data entry and database maintenance. - Maintain high standards of data quality and consistency. - Actively participate in process improvement initiatives, including adoption of automation and AI solutions. - Uphold confidentiality and comply with data protection regulations. **Key Responsibilities** - Screen patients and identify eligible cases for registry inclusion. - Obtain preliminary consent where required. - Collect and enter medical information into CRFs, electronic questionnaires, or paper-based forms. - Anonymise patient identifiers, reproduce, and upload results to secure platforms (e.g., SharePoint). - Coordinate data verification and validation activities with clinical teams. - Report discrepancies, data gaps, and quality issues to project leads. - Assist in the development and optimisation of data capture tools and procedures. - Participate in cross‑functional project meetings (clinical, research, IT, and AI teams). - Support the integration of new technologies to streamline data collection and enhance data integrity. **Required Skills** - Proficiency in data entry and handling structured electronic records (CRFs). - Basic understanding of clinical research methodology and terminology. - Familiarity with database tools and secure data transfer platforms (e.g., SharePoint, secure portals). - Strong attention to detail and commitment to data accuracy. - Ability to follow SOPs and maintain confidentiality under GDPR/EU data protection rules. - Good communication skills for liaising with clinicians, researchers, and IT staff. - Willingness to learn and apply emerging automation or AI tools in clinical data management. **Required Education & Certifications** - Bachelor’s degree in Medical Science, Nursing, Health Informatics, Clinical Research, or a related field. - Prior experience in clinical data collection, medical record management, or database entry is highly desirable. - Knowledge of Good Clinical Practice (GCP) guidelines is an advantage.
Strasbourg, France
On site
06-01-2026
Company background Company brand
Company Name
CHRU de Strasbourg - Hôpitaux Universitaires de Strasbourg
Job Title
Technicien d'étude clinique (H/F) - 100% - Base de données et registres Maladie de l'oeil
Job Description
Job Title: Clinical Study Technician – Eye Disease Database & Registry Role Summary: Support the collection, management, and quality assurance of clinical data for rare eye disease research. Perform manual data entry, screening, anonymization, and verification, while collaborating with multidisciplinary teams and contributing to the evolution of AI-based data capture tools. Expectations: - Accurately capture and enter data within deadlines. - Adhere to ethical, privacy, and regulatory standards (GDPR, SOX, HIPAA). - Communicate effectively with clinicians, lab staff, and project leads. - Demonstrate critical thinking to identify and resolve data discrepancies. - Proactively contribute to process improvements and tool development. Key Responsibilities: - Screen patients for eligibility; provide brief consent information when required. - Extract medical data from patient records into electronic Case Report Forms (CRFs), paper forms, or secure platforms (e.g., SharePoint). - Reproduce, anonymize, and transmit results to appropriate data repositories. - Organize and conduct data verification activities in preparation for monitoring visits. - Collaborate with AI/automation teams to refine data capture methodologies. - Maintain accurate logs of data entry, changes, and corrections. - Ensure timely and compliant submission of data to national and European rare disease registries (BNDMR, REDgistry). Required Skills: - Strong attention to detail and data integrity focus. - Proficiency with electronic data capture systems and MS Office suite. - Basic understanding of clinical trial terminology and data standards (e.g., CDISC). - Ability to interpret French medical documentation and maintain data confidentiality. - Excellent written and verbal communication. - Team player with adaptability to cross‑functional collaboration. - Problem‑solving orientation and willingness to learn AI/automation tools. Required Education & Certifications: - Bachelor’s degree in Life Sciences, Nursing, Medical Technology, or related field. - Prior experience in clinical data management or research data collection is preferred. - Knowledge of GDPR/clinical data protection regulations; certification in Clinical Research (e.g., GCP) is an advantage.
Strasbourg, France
On site
06-01-2026