Job responsibilities
Clinical/Scientific1) Deliver the clinical service of a section/subsection of the laboratory or designated area of work to nationally accepted standards (CPA/UKAS or equivalent) with appropriate technical support to include the following:a. Undertake or supervise the receipt, processing and analysis of samples;and the checking, interpretation and reporting of results (both standardand complex).b. Access relevant sources of information to aid interpretation of patientresults, including critical appraisal of the information.c. Collate patient and clinical information to assist and support future patient management.d. Interpret results with advice on further action for patient or familymembers, including calculation of risk where appropriate, within relevantprofessional guidelines2) Undertake appropriate complex or specialist technical and analytical procedures, as required, to process cells from a variety of biological specimens received which may be high risk (eg HIV, Hep C) and/ or derived from recognisable human or fetal parts. Work safely under exposure to toxic substances that are hazardous to health (eg PHA, colchicine)3) Undertake extended periods of analysis to identify genomic variation either through analysis of large data sets or examination of cytogenetic preparations4) Independently check and validate the analysis findings of other registered scientists, non-registered scientists and genetic technologists as appropriate, authorising repeat analyses or subsequent investigations in accordance with laboratory protocols. Identify unusual results and bring them to the attention of senior scientists for further discussion5) Interpret findings from the range of investigations undertaken on a patient. Undertake detailed literature review and interrogation of databases to investigate the clinical significance of genomic variation detected. Prepare reports withclinical interpretation within designated service areas for final authorisation by Senior Registered Clinical Scientists/Principal Scientists/Consultant Scientists6) Act in an advisory capacity to clinical colleagues on the submission of samples, appropriate tests and in the interpretation of results in designated areas of the service, under the supervision of the section head7) Supply a high level of scientific skill and expertise in the investigative procedures involved and take a high level of responsibility for his/her own work, subject to supervision from and the direction of, senior personnel in the laboratory. Be adaptable to changing diagnostic workload pressures, by making independent day-to-day decisions about own workload (e.g. prioritising own diagnostic cases or deciding when to undertake additional investigations). The post holder must communicate with, and when necessary obtain help/advice from, appropriate senior staff
8) Maintain up to date specialist level knowledge of current scientific literature and information (eg Professional Best Practice) for defined services in order to ensure that the designated services are of high quality9) Maintain proficiency in the use of complex software for the analysis of genomic samples10)Maintain proficiency in the navigation, interrogation and application of all relevant and up to date genome browsers/information databases (eg DGV, DECIPHER, Exome Variant Server and Alamut Visual) to assess significance of copy number variants and/or identified mutations and maintain up to date knowledge of scientific and clinical advances in the field.
Quality & Clinical Governance11)Work within the section/subsection to ensure achievement of and adherence to the standards required of an accredited laboratory, in close liaison with the Quality manager and under the direction of the section head and laboratory director.12)To ensure any identified risks are communicated to the appropriate personnel in line with laboratory and Trust protocols13)To ensure incidents are reported and investigated, including root cause analysis, in line with laboratory and Trust protocols14)Troubleshoot / maintain and improve existing services through knowledge of genetics and current advances in the field including communications with colleagues in other centres15)Participate in internal quality control, audit activities and internal and external quality assessment procedures16)Contribute within the team to improvements in efficiency and changes to clinical, scientific and technical protocols17)Participate in the preparation of the department for accreditation.18)To ensure that all members of staff based in the section abide by all statutoryrequirements, codes of practice, safety regulations and operational policies of the department and to be aware of these measures as applied to other sections.19)Implement laboratory record keeping processes and assist with retrieval and presentation of data as required20)Maintain confidentiality of information about patients, staff and other health service business in accordance with Data Protection Act of 1984.
Research & Development21)Contribute to planned and agreed research and service developments relevant to the aims of the department under the direction of senior scientists / Consultant Head of Laboratory. This may include using state of the art technologies to improve the efficiency of existing tests, transfer technology from research to diagnostics and to establish and implement new services. This may also include participation in formal funded research programmes22)Present laboratory findings from case studies, audit and research projects to local, national or international scientific meetings and in peer reviewed scientific journals23)Contribute to the design, validation and implementation of new assays/testing methodologies or continuous improvement of existing assays for the continued development of the service
Managerial24)Plan, manage and organise own workload to meet priorities and ensure timely reporting. Take responsibility for the accuracy of own work, undertake an appropriate proportion of the total workload of the Department and monitor own performance. The post holder will collaborate with all other staff, to be an effective team member, and achieve optimal use of resources25)To liaise with others on the day-to-day organisation of staff within the team and to ensure smooth running of the service overall26)Assist with the management of an additional component of the Genetics service (e.g. the supervision/training of designated staff, authorisation of competences, organisation of journal club, responsibility for EQA, delivery of routine audits)27)Through implementation of the Trust Core Values demonstrate a professional and responsible manner at all times.
Education & Development28)Participate in the teaching and training of Genetic Technologists, Pre-registration Scientists and other professional groups as required29)To actively participate in the departmental seminar programme, presenting as appropriate. This may extend to presenting data at scientific meetings.30)Participate in CPD activities, taking measures to acquire, improve and apply scientific skills and expertise to perform the job to a high level of skill; this includes rotation within the laboratory to build experience, attending internal and external training sessions, relevant courses and external study days, attendance at national or international scientific conferences and keeping up-to-date withcurrent scientific journals and literature through personal or group self-learning31)Participate in regular performance review and personal development planning
32)Undertake statutory and mandatory training in line with Trust protocols Human Resources33)Supervise the work of Genetic Technologists and any visiting students or healthcare professionals within the section as required
General34)Take responsibility with others for the daily maintenance of complexinstrumentation systems within the laboratory35)Take responsibility with others for the maintenance of stocks of reagents and consumables to ensure the proper functioning of the laboratory and efficient use of resources. Ensure that all equipment is used appropriately and safely and that any faults are reported for immediate rectification36)Abide by all Operational Policies applicable to the Department37)Co-operate with management and safety representatives in matters connected with the Health and Safety at Work Act of Practice for safety in laboratories38)Attend regular team, laboratory and departmental meetings and contribute to the development and implementation of departmental policies39)Participate in out of hours duties, if required, in line with the Department Out of Hours Policy40)Work such hours as required for the effective and timely performance of his/her duties, as specified in the terms of the contract of employment41)Undertake any other duties commensurate with experience and job role as a result of changes to the service as agreed by the Consultant Head of Laboratory or Trust and reviewed as part of the annual staff appraisal
