Lead Scientist (Diagnostic Cytopathology), Band 8a

To report at Consultant level by evaluating, reporting and authorising negative and positive non-gynae samples from urinary, respiratory and serous fluid systems, and FNA specimens. The level of reporting will be dependent on the qualification held. To perform primary screening of all other non gynae cytology samples, prior to Consultant reporting and authorisation. To participate in the Rapid On Site Assessment clinic. To participate in training of biomedical scientists and junior medical staff (one to one and group sessions.) To offer expert professional advice on the sampling and interpretation of specimens from urinary, respiratory and serous fluid systems. To liaise with Consultant colleagues within pathology and clinical staff delivering patient care. Attend MDTs as appropriate Write and update accordingly, Standard Operating Procedures (SOPs) for the department. Establish internal quality standards and that appropriate corrective measures are taken to ensure standards are maintained. Be conversant with the departments participation in external QA schemes and ensure prompt return of QA material and take appropriate measures as necessary to ensure standards are maintained. Job description Job responsibilities To report at Consultant level by evaluating, reporting and authorising negative and positive non-gynae samples from urinary, respiratory and serous fluid systems, and FNA specimens. The level of reporting will be dependent on the qualification held. To perform primary screening of all other non gynae cytology samples, prior to Consultant reporting and authorisation. To participate in the Rapid On Site Assessment clinic. To participate in training of biomedical scientists and junior medical staff (one to one and group sessions.) To offer expert professional advice on the sampling and interpretation of specimens from urinary, respiratory and serous fluid systems. To liaise with Consultant colleagues within pathology and clinical staff delivering patient care. Attend MDTs as appropriate Write and update accordingly, Standard Operating Procedures (SOPs) for the department. Establish internal quality standards and that appropriate corrective measures are taken to ensure standards are maintained. Be conversant with the departments participation in external QA schemes and ensure prompt return of QA material and take appropriate measures as necessary to ensure standards are maintained.