Luxembourg National Data Service (LNDS) is a brand of PNED G.I.E. an organisation created by the Luxembourg Government, to implement Luxembourg’s strategies in research, innovation, and digitalisation. LNDS enables value creation from secondary use of data, for public and private partners and supports the sharing and re-use of public sector data, in a trustable manner. The LNDS service portfolio includes know-how, capabilities, tools, infrastructure, and data services. Through efficient & responsible use of data and improving the secondary use of data, LNDS will support the acceleration of economic, ecological, and societal transitions. www.lnds.lu | LNDS on LinkedIn We participate in European project to support the secondary use of genomic data in the context of the European 1+ Million Genome (1+MG) initiative for an innovative and responsible ethical, legal and social implications (ELSI) framework. Our aim is to advise European policy makers in the implementation of a data infrastructure for secondary use of genomic data based on legal research, stakeholder interaction and translation of our findings into ethical, data protection and other legal norms into workable IT and policy solutions in the interest of society. LNDS plays a key role in several projects linked to the 1+ Million Genomes (1+MG) Initiative. As an ELSI Specialist, you will contribute to the privacy, ethical, legal, and regulatory dimensions of these strategic European initiatives. In this role, you will support LNDS's participation in 1+MG-related projects, ensuring compliance with relevant legal and regulatory frameworks while promoting the responsible use and sharing of genomic and health data. You will work closely with LNDS colleagues and collaborate with leading European stakeholders through working groups, expert networks, and project consortia. Analysis and interpretation of legal and/or ethical requirements based on legal and ethical norms, review of existing guidelines and, where applicable, case law for the challenges in secondary use of genomic data in the context of the 1+ Million Genome (1+MG) initiative. Pursuing ELSI by design and default, you will provide analyses of planned operations and workflows of secondary use as well as provide support on data protection impact assessments (DPIA). Development of policies and technical requirements frameworks to enable solutions for ELSI compliance for secondary use of genomic data in the context of European projects and the 1+ MG initiative. Development of or contribution to practical tools, templates, guidance, training and other instruments for ELSI compliance. Engagement in European working groups in the context of the 1+MG initiative, including preparation of content, formal documents, writing of minutes and interaction with the working group members. Engagement with relevant stakeholders, such as citizens, representative groups (consumer groups, patient associations etc.), data holders, data users, relevant ministries on the national and European level, data protection authorities as well as European bodies - such as the European Commission or the EDPB -, and contribution to consensus building