Explore opportunities 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 professional 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.