ERN-EYE started its activities the 1st March 2017. Since then, our activities grew up and new needs appeared.
Please find here the open positions in ERN-EYE and join us to serve better care for Rare Diseases in Europe!
Within the Project Management Team
ERN-EYE is recruiting a Project Officer
As part of ERN-EYE, the European project RealiseD, in which the project officer will be primarily involved, aims to improve the methodological and operational approach to clinical trials in rare and ultra-rare diseases. Launched in early 2025, the project brings together more than 50 partners from academia (including two ERN-EYE members, Strasbourg University Hospitals and Ghent University Hospital), industry, patient associations, and regulatory agencies, and will run until 2029. RealiseD will promote the development and acceptance of innovative methods for trial design, as well as for data (re)use, analysis, and interpretation. These resources will be integrated into practical guidelines and digital tools designed to facilitate the implementation and conduct of innovative trials.
Mission
The project officer collaborates with network physicians and all stakeholders to coordinate RealiseD and implement ERN-EYE-related activities within the project, mainly under WP2. The research project officer will manage activities related to clinical study design methodologies for rare eye diseases, including the organization of data collection, as well as regulatory, financial, and organizational aspects.
This position will focus on:
- Planning and monitoring activities related to methodologies relevant to clinical research in rare eye diseases, drafting ad hoc documents, and ensuring compliance with project deadlines.
- Compiling, standardizing, and monitoring the analysis of existing data in the field, drawn from registries, databases, and existing trials, in order to generate insights on current practices.
- Organizing and facilitating exchanges within ERN-EYE among the various project stakeholders (clinicians, methodologists, biostatisticians, patient representatives, industry partners, etc.) across different countries.
- Contributing to the design of patient-centered outcomes (PCOMs; quality of life) and to the development of clinical trial protocols tailored to the specificities of rare diseases, in close collaboration with clinicians, methodologists, patient representatives, and industry partners.
- Participating in the drafting of scientific documents, methodological guidelines, and materials for disseminating results.
Do not hesitate to contact us if you need additional information : isabella-anna.vacchi@chru-strasbourg.fr