[ref. w43998201] Clinical Research Practitioner
NHS Jobs Chippenham
Job Summary: To assess, plan and monitor care for patients as part of a clinical research team. To act as an advocate for staff, participants and their relatives at all times. Keep abreast of innovations and developments in research governance, ethics and other regulatory and legal guidelines governing clinical research.
To support research across clinical specialities including diabetes, neurological, cardiovascular, respiratory, vaccines, mental health, and community-based care. To help identify patients eligible for research projects, and recruit patients into clinical trials or studies.
To support the practice to ensure compliance with its statutory and regulatory obligations, such as but not limited to the Care Quality Commission and Data Protection Act 2018(GDPR) Principal Activities Clinical Research Assist in maintaining electronic databases and paper records, to ensure that patients schedules to have follow-up visits are not overlooked and have fulfilled all study assessments according to the protocol.
Assist in ensuring all documentation is filed in a timely manner and ready for inspection. Assist with inspections as required. Arrange couriers/post for clinical research samples. Support the research team with general tasks, as required. Possess IT skills Word, PowerPoint and familiar with email correspondence.
To directly communicate with patients on matters relating to their ongoing and highly complex health needs giving due consideration to the likelihood that there will be emotive issues which will require developed skills of tact, diplomacy, and empathy.
To ensure that patients have detailed assessments made of their healthcare needs and that individual programmes of care are planned, implemented, and regularly reviewed. Facilitate patient referrals to appropriate clinical services. To maintain and promote the safeguarding of all patients and their families/carers.
Respond to medical emergencies. Ensure that the principles of Infection Control are always adhered to. Provide information and support for patients involved in research projects. Responsible for ensuring patients treatments, assessment, follow-ups, and data collection is co-ordinated and processed according to the appropriate research protocols.
This will include close liaison with research teams, appropriate Research & Development Departments and with Clinical Nurse Specialists. To support study set up including assisting with preparation of documents and authorisations. To actively promote research amongst clinicians, service users, carers, and the wider NHS.
Taking responsibility for the management, co-ordination, and facilitation of concurrent research studies. To provide clinical support and expertise on NIHR portfolio research projects. Principal Activities Education and Development To keep abreast of advances in clinical practice and identify personal training and development needs.
Support junior colleagues in their development by encouragement, informal teaching and coaching. To attend meetings as directed by the Nurse manager or Trials lead, member of the senior management team and/or partners. To attend mandatory training identified through the appraisal system.
Attend investigation meetings and site initiation visits to ensure an in-depth knowledge of all study protocols. Maintain own training records. Principal Activities Professional Contribute and work within the broad framework of the clinical governance agenda.
Ensure that communication is effective between all stakeholders giving adequate attention to the complex and sensitive nature of such information. Make all reasonable attempts to overcome any barriers to understanding that may occur, giving due consideration to ethnicity, language, educational ability, barriers caused by illness/distress etc.
which may adversely affect communication. To work in a flexible manner to meet the needs of the service and as directed by senior staff and GPs. Participate in the review of significant and near miss events applying a structured approach. Principal Activities Administrative Follow practice, ICB, ICH, NHS England and sponsor company policies, procedures, and guidelines.
Complete reports and forms required by the practice, ICB and NHS England Participate in staff surveys and contribute to research-based practice. Ensure all equipment and drugs with expiry dates are in date. Research Ensure that any data collection is conducted according to specific research protocols (in liaison with the research teams) and adheres to the Data Protection Act 2018 and according to Good Clinical Practice guidelines.
Adherence to and interpretation of research study protocols and standard operating procedures including compliance with local, national, and where appropriate, international research regulations. To assist participants with the completion of questionnaires as necessary.
To take relevant patient samples for clinical trials, such as blood samples, package and dispatch as per defined protocols, where appropriate. Maintain accurate patient trial documentation, complete Case Record Forms, including the use of electronic data capture systems and ensure relevant information is recorded in patients medical notes.
To support research across clinical specialities including diabetes, neurological, cardiovascular, respiratory, vaccines, mental health, and community-based care. To help identify patients eligible for research projects, and recruit patients into clinical trials or studies.
To support the practice to ensure compliance with its statutory and regulatory obligations, such as but not limited to the Care Quality Commission and Data Protection Act 2018(GDPR) Principal Activities Clinical Research Assist in maintaining electronic databases and paper records, to ensure that patients schedules to have follow-up visits are not overlooked and have fulfilled all study assessments according to the protocol.
Assist in ensuring all documentation is filed in a timely manner and ready for inspection. Assist with inspections as required. Arrange couriers/post for clinical research samples. Support the research team with general tasks, as required. Possess IT skills Word, PowerPoint and familiar with email correspondence.
To directly communicate with patients on matters relating to their ongoing and highly complex health needs giving due consideration to the likelihood that there will be emotive issues which will require developed skills of tact, diplomacy, and empathy.
To ensure that patients have detailed assessments made of their healthcare needs and that individual programmes of care are planned, implemented, and regularly reviewed. Facilitate patient referrals to appropriate clinical services. To maintain and promote the safeguarding of all patients and their families/carers.
Respond to medical emergencies. Ensure that the principles of Infection Control are always adhered to. Provide information and support for patients involved in research projects. Responsible for ensuring patients treatments, assessment, follow-ups, and data collection is co-ordinated and processed according to the appropriate research protocols.
This will include close liaison with research teams, appropriate Research & Development Departments and with Clinical Nurse Specialists. To support study set up including assisting with preparation of documents and authorisations. To actively promote research amongst clinicians, service users, carers, and the wider NHS.
Taking responsibility for the management, co-ordination, and facilitation of concurrent research studies. To provide clinical support and expertise on NIHR portfolio research projects. Principal Activities Education and Development To keep abreast of advances in clinical practice and identify personal training and development needs.
Support junior colleagues in their development by encouragement, informal teaching and coaching. To attend meetings as directed by the Nurse manager or Trials lead, member of the senior management team and/or partners. To attend mandatory training identified through the appraisal system.
Attend investigation meetings and site initiation visits to ensure an in-depth knowledge of all study protocols. Maintain own training records. Principal Activities Professional Contribute and work within the broad framework of the clinical governance agenda.
Ensure that communication is effective between all stakeholders giving adequate attention to the complex and sensitive nature of such information. Make all reasonable attempts to overcome any barriers to understanding that may occur, giving due consideration to ethnicity, language, educational ability, barriers caused by illness/distress etc.
which may adversely affect communication. To work in a flexible manner to meet the needs of the service and as directed by senior staff and GPs. Participate in the review of significant and near miss events applying a structured approach. Principal Activities Administrative Follow practice, ICB, ICH, NHS England and sponsor company policies, procedures, and guidelines.
Complete reports and forms required by the practice, ICB and NHS England Participate in staff surveys and contribute to research-based practice. Ensure all equipment and drugs with expiry dates are in date. Research Ensure that any data collection is conducted according to specific research protocols (in liaison with the research teams) and adheres to the Data Protection Act 2018 and according to Good Clinical Practice guidelines.
Adherence to and interpretation of research study protocols and standard operating procedures including compliance with local, national, and where appropriate, international research regulations. To assist participants with the completion of questionnaires as necessary.
To take relevant patient samples for clinical trials, such as blood samples, package and dispatch as per defined protocols, where appropriate. Maintain accurate patient trial documentation, complete Case Record Forms, including the use of electronic data capture systems and ensure relevant information is recorded in patients medical notes.
Coordinate treatment, assessment, and follow-up as necessary in accordance with Research protocol
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prior to commencement of the study. Work with the R+D department in contract negotiations Liaise with the NIHR Clinical Research Network throughout the study and facilitate the lines of communication between the Trust / R+D and the NIHR CRN.
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University Hospitals Bristol and Weston NHS Foundation TrustBristol, 19 mi from Chippenham (Wiltshire)
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