Explore prospects as a Clinical Scientist focusing on rare diseases at Oxford University Hospitals NHS Foundation Trust, analyzing complex genomic data. This role emphasizes both independent work and collaborative research. As part of our rare disease and cancer team, you will contribute significantly to diagnostic testing and research initiatives.

The position demands a keen understanding of molecular and cytogenetic investigations, as well as the ability to mentor train pre-registration Clinical Scientists.

Your role ensures high-quality patient care through careful analysis and reporting of results. Key Responsibilities:
Facilitate clinical services maintaining national quality standards
Oversee sample processing and result interpretation




Conduct and review complex genetic analyses
Provide expert advice on test recommendations
Engage in teaching and support skilled growth Requirements:
HCPC registration essential for band 7, or training completion for band 6
Proficient in genomic analysis and relevant software
Demonstrated analytical and communication skills
Team-oriented mindset for multidisciplinary teamwork
Openness to continuous learning and adaptation Harness your analytical capabilities and contribute to pioneering healthcare solutions at Oxford University Hospitals.

📌 Oxford Clinical Scientist Rare Diseases Cape Breton Island (Canada)
🏢 Allscreens Nationwide
📍 Canada