Principal Clinical Scientist Rare Disease Genomics
Cambridge University Hospital NHS Foundation Trust
The Cambridge Genomics Laboratory, Lead Laboratory for the East Genomic Laboratory Hub, is looking to recruit a Principal Clinical Scientist (Band 8A).
We are seeking an enthusiastic, self-motivated Clinical Scientist with scientific and operational experience of genomics laboratory testing to lead and manage a team. You will have extensive experience of analysing and interpreting genomic results alongside preparing and authorising clinical reports. You will have excellent communication, leadership, management and supervisory skills. You will be responsible for delivering a high quality service and expected to liaise closely with clinical colleagues and technical team members. You will be a key member of the rare disease management team and be responsible for the day-to-day delivery of a part of the rare disease service within the Cambridge Genomics Laboratory. In addition, you will contribute to quality management activities, including compliance with laboratory accreditation standards, alongside teaching and training commitments. You should hold HCPC registration as a Clinical Scientist.
Main duties of the job
Responsible for leading and managing a team of scientists undertaking genetic diagnostic tests in rare disease.
Analysis, interpretation of data, and writing and authorising of clinical reports.
Providing clinical scientific expertise for the repertoire of disorders/tests offered by the assigned team.
Training and mentoring of scientific staff.
Member of the laboratory leadership team, contributing to all aspects of providing a high quality service.
Person Specification
Qualifications
* Registered Clinical Scientist with HCPC
* Completion of a formal training programme in Laboratory Genetics, OR postgraduate qualification (PhD or equivalent) in relevant subject and externally assessed clinical genetics laboratory experience
* Completion of Part 1 FRCPath in Genetics; OR PhD in relevant Human Genetics subject and actively preparing for Part 1 FRCPath
* Part 2 FRCPath in Genetics, or working towards
* Undergraduate degree in an appropriate biological science
Experience
* Significant experience of working as a Clinical Scientist in a genomics laboratory
* Experience of research and development relevant to genomic testing
* Experience of project management
* Experience of management and supervision of staff
Skills
* Analysis of Rare Disease genetic test results
* Able to organise and manage complex activities
* Able to provide leadership and training to scientific teams within the department
* Able to maintain intense concentration on important tasks despite frequent interruptions
* Excellent verbal and written communication skills
* Able to use and manipulate lab computer systems and standard software packages
* Able to prepare and present complex scientific and clinical information at meetings or as part of teaching/training events
* Able to develop new policies and protocols
Additional Requirements
* The ability to understand and behave at all times, towards patients, visitors and colleagues according to the Trust values of Safe, Kind, Excellent.
Knowledge
* Comprehensive knowledge of human genetics
* Comprehensive knowledge and understanding of Rare Disease cytogenetics and molecular genetic techniques
* Experience and knowledge of analytical methods, problem solving and troubleshooting
* Good knowledge of general managerial procedures
* Knowledge of data protection requirements
* Thorough knowledge of requirements of UKAS ISO:15189 and understanding of quality assurance
Disclosure and Barring Service Check
This post is subject to the Rehabilitation of Offenders Act (Exceptions Order) 1975 and as such it will be necessary for a submission for Disclosure to be made to the Disclosure and Barring Service (formerly known as CRB) to check for any previous criminal convictions.
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