About this role

<h2>About Congenica, a SeqOne Company</h2>Congenica, a SeqOne company, develops next-generation genomics software that turns complex sequencing data into clear, actionable insights for clinicians and researchers. Our platforms power high-impact applications in oncology and rare disease, with a strong focus on robustness, reproducibility, and speed. We are building a world-class team in Montpellier (FR), Paris (FR), and Cambridge (UK).<h2>Why SeqOne?</h2><ul><li>Direct Impact: Your contributions will enhance customer experience and shape the evolution of our genomic products.</li><li>Stimulating Environment: Passionate team, innovative projects, and a culture of transparency.</li><li>Flexibility: Remote work options, flexible hours, and competitive benefits.</li><li>Growth Opportunities: Internal career development, continuous training, and participation in scientific conferences.</li><li>Soft Skills: "Unstoppable Positivity" (resilience and solution-first mindset) and "Open Heart, Hands-On" (kindness combined with direct feedback).</li></ul>We are expanding our network Clinical Scientist team as part of our clinical interpretation service, and are looking for experienced rare disease genomics scientists to join us on a flexible basis, with ad hoc, part-time and full-time hours available. We are keen to hear from candidates who can start as soon as possible.<h2>Tasks</h2><ul><li>Genomic Interpretation: Analyse and interpret next-generation sequencing (NGS) data, whole exome sequencing (WES), and whole genome sequencing (WGS) for rare disease diagnostics.</li><li>Variant Classification: Apply evidence-based clinical standards and guidelines to classify genetic variants.</li><li>Quality, Compliance & Regulatory Standards: Work within an IVDR-regulated clinical interpretation platform alongside FRCPath and HCPC- registered Clinical Scientists, upholding the highest standards of genomic analysis, reporting and governance.</li><li>Collaboration: Work alongside NHS and industry partners, clinicians, bioinformaticians, genomic experts and Clinical Scientists - all united by a shared commitment to putting patients at the heart of every diagnostic decision.</li><li>Quality & Development: Contribute to enhancing our clinical interpretation services and platform development, underpinned by ISO standards, top EQA performance and a commitment to clinical safety.</li></ul><h2>Requirements</h2><ul><li>HCPC registration (or equivalent)</li><li>Hands-on experience in WES/WGS analysis and diagnostic report writing</li><li>Up-to-date working knowledge of ACMG/ACGS variant classification guidelines</li><li>Current and/or previous experience using the Congenica platform (preferred)</li></ul><h2>Benefits</h2><ul><li>Fully remote and flexible working (indemnity insurance incl)</li><li>Variable hours to suit your availability - from ad hoc through to full time</li><li>The opportunity to work within an established clinical interpretation service</li><li>Compensation depends on experience, with a rate of EUR 35–80 per hour</li><li>Flexible number of hours</li></ul>