Senior Research Assistant Practitioner

For further information on this role, please see the attached detailed Job Description and Person Specification. • Work autonomously screening patients suitability for entry into research studies, by attending MDTs and clinics or searching patient case notes exercising judgment and knowledge of trial eligibility criteria. • Be familiar with the application processes involved in the submission to the appropriate Ethics and R&D Committees by the Clinical Trial Coordinators/ Senior Trial Coordinators. • Identify patients that may be suitable for research projects and initiate discussion with patients and carers about defined research protocols. • Ensure patients are fully informed prior to entry into a research study and that all information is understood. • Develop tumour site-specific knowledge in order to enhance practice. • Provide support and reassurance to patients, referring them to the appropriate units or teammembers as necessary. • To complete Good Clinical Practice (GCP) and HTA training and adhere at all times to regulations as described in Good Clinical Practice, and to the most current guidance relating to Research Governance and Research Ethics in each Trust. • To recognise own limitations and undertake both mandatory and specialist training to ensure compliance with all clinical research regulatory frameworks. • To act as an advocate for staff, patients and relatives at all times. • To ensure the benefits to patients are maximised through careful, economical and appropriate use of NHS resources including equipment, property, money, time etc. • To promote a safe clinical environment for all patients, visitors and staff. • To assist with any local or trust initiatives to ensure the continuous improvement of the quality of services and safeguarding of high standards of care. Job description Job responsibilities For further information on this role, please see the attached detailed Job Description and Person Specification. • Work autonomously screening patients suitability for entry into research studies, by attending MDTs and clinics or searching patient case notes exercising judgment and knowledge of trial eligibility criteria. • Be familiar with the application processes involved in the submission to the appropriate Ethics and R&D Committees by the Clinical Trial Coordinators/ Senior Trial Coordinators. • Identify patients that may be suitable for research projects and initiate discussion with patients and carers about defined research protocols. • Ensure patients are fully informed prior to entry into a research study and that all information is understood. • Develop tumour site-specific knowledge in order to enhance practice. • Provide support and reassurance to patients, referring them to the appropriate units or teammembers as necessary. • To complete Good Clinical Practice (GCP) and HTA training and adhere at all times to regulations as described in Good Clinical Practice, and to the most current guidance relating to Research Governance and Research Ethics in each Trust. • To recognise own limitations and undertake both mandatory and specialist training to ensure compliance with all clinical research regulatory frameworks. • To act as an advocate for staff, patients and relatives at all times. • To ensure the benefits to patients are maximised through careful, economical and appropriate use of NHS resources including equipment, property, money, time etc. • To promote a safe clinical environment for all patients, visitors and staff. • To assist with any local or trust initiatives to ensure the continuous improvement of the quality of services and safeguarding of high standards of care.