[Hiring] Clinical Scientist @SeqOne

Role Description

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.

• Genomic Interpretation: Analyse and interpret next-generation sequencing (NGS) data, whole exome sequencing (WES), and whole genome sequencing (WGS) for rare disease diagnostics.
• Variant Classification: Apply evidence-based clinical standards and guidelines to classify genetic variants.
• 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.
• 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.
• 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.

Qualifications

• HCPC registration (or equivalent)
• Hands-on experience in WES/WGS analysis and diagnostic report writing
• Up-to-date working knowledge of ACMG/ACGS variant classification guidelines
• Current and/or previous experience using the Congenica platform (preferred)

Benefits

• Fully remote and flexible working (indemnity insurance incl)
• Variable hours to suit your availability - from ad hoc through to full time
• The opportunity to work within an established clinical interpretation service
• Compensation depends on experience, with a rate of EUR 35–80 per hour
• Flexible number of hours

Company Description

SeqOne is a leading and fast-growing clinical genomics company committed to making personalized medicine a reality for every patient. Our AI-powered NGS platform and expert services help molecular laboratories turn genomic data into clinical answers faster, supporting variant interpretation and reporting across rare and inherited diseases, oncology, preventive genomics, and infectious diseases. Founded in 2017, SeqOne is IVDR certified and used by public and private labs and national genomic programs in over 35 countries.