Clinical Scientist Clinical Biochemistry (band 8a)

Keighley, ENG, GB, United Kingdom

Job Description

To provide a comprehensive scientific service (analytical and advisory) to medical and other healthcare professionals within Airedale NHS Foundation Trust and primary care users of the service.



Maintaining up to date highly specialised knowledge and providing biochemical advice to users of the service, under the direction and leadership of the Consultant Clinical Scientist.



To attend the Biochemistry Clinical Group and contribute towards setting department policy on service provision and developments.



To deputise for the Consultant Clinical Scientist and Principal Clinical Scientist, where appropriate.



To be registered as a Clinical Scientist with the Health & Care Professions Council and as an independent practitioner work within its rules and regulations, the national guidelines of the profession and UKAS. To work under the direction of the Consultant Clinical Scientist and be an autonomous practitioner capable of dealing professionally with clinical colleagues including medical and nursing staff. To provide clinical & scientific leadership, ensuring that all departmental staff and clinical users focus on quality and patient safety.

We are delighted to offer a wide range of benefits to employees including:



Cycle to Work



Travel Scheme



Childcare Vouchers with Salary Sacrifice



Onsite Nursery



Buying and Selling Annual Leave



Car Leasing



Employee Assistance Programme



Employee Health and Wellbeing



Extensive Reward Scheme



Counselling Service



Financial packages including Vivup and Wagestream



Staff Networks, Enable, Rainbow, Gender, Race Equality Ecoaware & Admin Network.



Our values:



We understand that it's down to the hard work, effort and dedication of our staff that makes a difference for our patients. Our people really do make our Airedale experience - we take pride in fostering a friendly, effective and caring work environment. Our values are part of our DNA, which are:



Committed to Quality of Care



Compassion



Working together for patients



Improving Lives



Everyone Counts



Respect and Dignity



Got questions before you apply, please contact the recruiting manager to find out more.



To be registered as a Clinical Scientist with the Health & Care Professions Council and as an independent practitioner work within its rules and regulations, the national guidelines of the profession and UKAS.



To work under the direction of the Consultant Clinical Scientist and be an autonomous practitioner capable of dealing professionally with clinical colleagues including medical and nursing staff. To provide clinical & scientific leadership, ensuring that all departmental staff and clinical users focus on quality and patient safety. To be able to offer advice regarding patient management based on specialist knowledge, expertise and best practice examples. To deputise for the Consultant Clinical Scientist and Principal Clinical Scientist, as appropriate To undertake CPD activities, maintain and demonstrate competence in all areas of practice. To discuss with and advise medical staff, including senior clinicians, on the clinical interpretation of biochemistry investigations. To work with a degree of autonomy and to recommend further action based on the clinical and biochemical information, such as a change in treatment or referral for additional investigations. To instigate further testing based on results already available. To participate in the regular review of all biochemistry assay methods utilised within the department. To contribute to the development and implementation of policies and protocol To contribute to the selection and procurement of analytical equipment in the laboratory To propose and implement changes to working practices including the introduction of new tests. To propose and help manage the introduction of new services. To conduct clinical audit and contribute towards the development of best practise. To attend and contribute to departmental meetings related to management, service development and policy development. To ensure the repertoire of tests available is up to date, appropriate and meets the requirements of evidence-based practise. To undertake reporting, investigation, and follow-up of adverse events Where appropriate, to represent the department at meetings with users to discuss the biochemistry service and to plan further developments, for instance in response to new national initiative and guidelines. Where appropriate to take delegated responsibility for ensuring the implementation of trust-wide and departmental policies. To work jointly with colleagues from other trusts where specialist investigations required that are not carried out within the trust. To advice clinical staff on the best use and limitation of these specialist tests. To ensure that all clinical incidents and complaints are reported, investigated and used to improve practice, in line with Trust policies, procedures and national guidelines. To use the laboratory database and associated software to locate appropriate patient & laboratory data, provide interpretation and resolve and correct erroneous information, compiling and analysing statistics and prepare clinical and scientific presentations.

Training



To provide day to day clinical and scientific leadership and training to staff in specific areas and Pathology in general. To provide undergraduate and postgraduate medical teaching sessions to medical, nursing and laboratory staff as necessary To supervise and provide in-service training to Biomedical Scientists towards their required professional qualifications. To participate regularly in departmental clinical case discussions and seminars.

Management



In conjunction with the clinical lead for blood sciences plan and organise a range of activities and projects in the department. Some of these may require working over prolonged periods of time to complete, some extending into several years and requiring regular reviews of progress and adjustment of plans. In conjunction with the clinical lead for Consultant Clinical Scientist and General Manager/Cross-site Service Lead, to provide leadership and guidance in the development and selection of analytical methods employed. To liaise with other departments, within and outside pathology, and commercial companies, to achieve success in the planning process. Where complaints arise from patients, clinicians and other users of the service, to deal in conjunction with the clinical lead for blood sciences with the immediate problems, resolving conflict where possible and to suggest possible actions that are required to the Head of Department. Monitor laboratory performance in external quality assessment schemes. Work with the national organisers of these when there are problems identified with laboratory performance.

Communication



To communicate with patients where necessary to discuss tests and test results, some of which are highly specialised. To communicate with clinical colleagues on a range of patient related issues, often involving the discussion of specialist tests. To disseminate knowledge derived from research or private study. This may be achieved by presentation at local, regional or national meetings; or by publication in peer reviewed journals. To participate regularly in departmental meetings To give presentations to laboratory staff including consultants, and biomedical staff. To ensure that all staff within the department are aware of any changes to practice or procedures that fall within their sphere of responsibility. To communicate with colleagues within the department on a range of scientific and clinical subjects. To co-operate and consult with medical, scientific, and clerical staff throughout Pathology to ensure adequate lines of communication, to resolve problems and help determine strategies for development of the service. To organise and participate in meetings to this end as appropriate.

Research & Development / Audit



To carry out testing and evaluation of new equipment as required To plan, organise and participate in research and development projects and where appropriate involve clinical colleagues from other disciplines. To advise clinical colleagues on their research when it involves biochemistry, and to contribute to these projects when appropriate. To undertake Clinical Audit of service effectiveness with colleagues within pathology at local, regional, and national level and contribute to discussions on clinical audit in other medical specialities. To prepare project plans and negotiate funding from external/ internal sources to ensure project completion. To use evidence-based practice, clinical audits, and published research to improve the service. To originate, plan, undertake and report on audit topics including both clinical and laboratory audits that are appropriate for the department. To work jointly with clinicians and other staff outside clinical biochemistry who are undertaking audit which involve aspects of the biochemistry service.

General Duties



The jobholder will undertake other duties commensurate with the grade as agreed with senior management. The duties and responsibilities of the job will be reviewed as part of staff appraisal. * This job description is an outline of the current position and may be amended in detail or emphasis in the light of the future requirements of the service.

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Job Detail

  • Job Id
    JD3347100
  • Industry
    Not mentioned
  • Total Positions
    1
  • Job Type:
    Full Time
  • Salary:
    Not mentioned
  • Employment Status
    Permanent
  • Job Location
    Keighley, ENG, GB, United Kingdom
  • Education
    Not mentioned