Ic32_24 Genomics Data Curator - Barcelona - Data Bene

    Data Bene
    Data Bene Barcelona

    hace 1 semana

    Default job background
    Descripción

    We are seeking a Bioinformatician to perform data harmonisation and curation activities, data quality assurance, and bioinformatics support. The selected candidate will coordinate tasks between research groups involved in the precision medicine national programme IMPaCT.

    About the Project

    The project involves implementing a screening tool to improve prevention, diagnosis, and treatment of neurodevelopmental psychiatric disorders, using the 22q11.2 deletion syndrome (22q11.2DS) as a model.

    This is a pilot project supported by the Network of Genomic Analysis Centers of IMPaCT-Genomic Medicine.

    Tasks and Responsibilities

    • Data harmonisation activities in alignment with IMPaCT
    • Establish a data dictionary of variables using suitable ontologies
    • Support database development and maintenance (clinical and genomic data)
    • Coordinate data collection, quality checks, and generation of metadata
    • Support genomic analysis plans and curation of results
    • Presentations internally and to external stakeholders to update progress and status of curation activities

    About the Centre for Genomic Regulation

    The Centre for Genomic Regulation (CRG) is an international biomedical research institute of excellence, based in Barcelona, Spain, with over 400 scientists from 44 countries.

    About the EGA

    The European Genome-Phenome Archive (EGA) is a resource for permanent secure archiving and sharing of all types of potentially identifiable bio-molecular, phenotypic, and clinical data resulting from biomedical research projects.

    Candidate Profile and Requirements

    We are looking for a candidate with a degree in Biology, Biomedicine, or equivalent, combined education and/or experience in Bioinformatics or Data Science.

    • Good understanding of clinical concepts and genomics
    • Motivation, creativity, initiative, and proactive attitude
    • Experience with high-throughput genomic and clinical data curation, harmonization, quality control checks, and analysis
    • Experience with health data standards (OMOP, FHIR…)
    • Experience with the use of ontologies/vocabularies (LOINC, SNOMED…)

    Selection Procedure

    The selection procedure includes:

    • Evaluation of CVs up to a maximum score of 40 points
    • Cover Letter with a maximum length of 2500 characters with spaces (maximum score of 20 points)
    • Personal interview with a maximum score of 40 points

    Labor Conditions

    The position is full-time (40h/week) with a temporary contract (1 year and three months approximately, linked to the PMP CESPED project), financed by recovery, transformation, and resilience funds from the European Union.

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