Clinical Research

• Analyse and interpret next-generation sequencing (NGS) data, whole exome sequencing (WES), and whole genome sequencing (WGS) for rare disease diagnostics
• Apply evidence-based clinical standards and guidelines to classify genetic variants
• Work within an IVDR-regulated clinical interpretation platform alongside FRCPath and HCPC-registered Clinical Scientists
• Collaborate with NHS and industry partners, clinicians, bioinformaticians, genomic experts and Clinical Scientists
• Contribute to enhancing clinical interpretation services and platform development
• Uphold quality, compliance, regulatory, governance and clinical safety standards
• Support diagnostic decisions centered on patients

Explore Clinical Scientist – Rare Disease Genomics at SeqOne. Review requirements and application details.