ECH Santé supports medical institutions with all the tasks related to clinical trials. Our motto: LET THE HEALTHCARE PROVIDERS FOCUS ON THEIR PATIENTS
Clinical trials represent an opportunity for patients care, but the administrative complexity can be a burden for the medical staff. ECH Santé supports your trials so that clinical research remains an asset for the patients and their healthcare providers:
- Data entry into the study CRF.
- Coordination with the sponsors / administrative paperwork
- Rationalisation des tâches liées à la recherche clinique à l’échelle de l’établissement
- team coordination
- préparation des documents d’aide au recueil de données
- worksheets
- staff training and protocole follow-up
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Extensive experience in the different areas of medical research (regulation, monitoring, coordination)
Guy Teissier, managing director
- 6+ years clinical research experience within international Clinical Research Organizations
- Monitoring/coordination of Phase I to III trials within numerous therapeutic areas (Oncology, Cardiology, Endocrinology, Neurology, Hematology...)
- Expérience sur des études complexes (pédiatriques, génétiques)
- International standard expertise in ICH-GCP and local regulations IT proficiency and workflow optimization
- IT Proficiency and workflow optimization skills
- Relationship skills with investigators and medical staff
English (UK)
Français