At a Glance
- Tasks: Lead surgical and oncology clinical trials, ensuring high-quality care for patients and staff.
- Company: Join Ashford & St. Peter's Hospitals NHS Foundation Trust, a leading healthcare provider in Surrey.
- Benefits: Enjoy competitive salary, NHS benefits, and opportunities for professional development.
- Other info: Dynamic work environment with a focus on collaboration and continuous learning.
- Why this job: Make a real difference in patient care while advancing your career in clinical research.
- Qualifications: Degree in nursing or related field; experience in clinical research is a plus.
The predicted salary is between 41957 - 50387 £ per year.
The postholder will be responsible for the organisation and day to day running of surgical and oncology clinical trials at Ashford & St Peters NHS Hospital Trust. Support and assist with the general activities and research trials within the designated department. Provide a high quality of service and care for staff and patients, external organisations and institutes involved in research activities. Provide advice and support for patients and health care staff regarding the on-going care of research participants. Be a resource within the Trust regarding advice and information on the clinical trials.
Main duties of the job:
- Working autonomously
- Manage own time and workload
- Plan, deliver and evaluate patient-centred care, including providing research based evidence to develop clinical policies and practice
- Measure and record treatment outcomes
- Request and interpret results of various tests
- Make independent professional decisions and be accountable for them
- Manage patient clinics within a study's requirement
- Inform study patients' GPs of their participation in a clinical trial, liaising with the GP as necessary
Key working relationships:
- Acute Medical/Surgical/Oncology Teams
- R & D team
- Externally: R & D teams in other NHS Trusts and organisations, KSS CRN
Key Result Areas:
- Support the R&D department with the effective running and recruitment of Surgery and Oncology related trials
- Provide regular training and support to clinical staff regarding the medicine trials, including dissemination of results of trials to improve evidence based practice
Professional Responsibilities:
- Practice in accordance with Professional Practice
- Ensure that the study is conducted adhering to the International Conference for Harmonisation (ICH) and Good Clinical Practice (GCP) guidelines, UK Clinical Trials Regulations and in accordance with its protocol
- Ensure safety and confidentiality of information regarding patients
- Show evidence of on-going professional development
- Maintain awareness of and comply with all statutory and Trust Policies, Procedures and Guidelines
- Be conversant with information technology in use within the Trust and as required by the studies
- Provide out of hours advice and assistance in relation to on-going research patient care
- Maintain appropriate clinical competences, keeping updated with current practice and maintaining a professional portfolio
- Promote and maintain good working relationships with all departments within the trust
- Support staff within the department, advising and liaising as required
- Provide on-going support and encouragement to all research participants throughout their involvement in the study
- Maintain professional links with other departments within the Trust
- Assist with Study days and other teaching events
Education, Information and Reporting:
- Maintain own personal and professional development
- Act as a resource for others and keep up to date with developments in research
- Work with senior colleagues in preparing reports or submissions to the Research and Development department and/or Ethics Committees
- Involvement in producing progress reports of ongoing trials to the wider research team and clinical teams within maternity and gynaecology
- Involvement in the dissemination process following completion of a research study
- Regular training/teaching/presenting of research trials to clinical staff
- Regular mentoring/teaching of students
Leadership or managerial:
- Act as a role model to less experienced members of the research team
Technology or system support:
- Use the Trust computer systems, ICE, PowerChart, Somerset, PACS to document and follow up patient care
- Complete case report forms, ensuring that all source documents are accurately maintained
- Assist Clinical Research Monitors with data verification and queries
Communications and Engagement:
- Ensure an in-depth knowledge of study protocols and specific medical conditions, including but not limited to specialties such as Diabetes, Cardiovascular disease, IBD, Rheumatology, Respiratory and Neurology
- Maintain good communications with all staff so that they are fully supported in their study role
- Identify and screen for potential research participants, assessing suitability according to eligibility criteria/requirements, including judgement of suitability to participate in a study
- Advise and support patients and their families when considering participation in a study
- Teach, advise and support medical and nursing staff about the studies so that they can identify, recruit, administer study drugs and care for study patients according to the specific protocol requirements
- Ensure availability of clear and easy to follow study guidelines, so that staff workload is kept to a minimum
- Be available to advise on patients being screened for study enrolment, both acute inpatient and long-term out-patients studies
- Assist and, when appropriate, be responsible for consent and randomisation procedures
- Monitor for and send expedited severe adverse event forms, where necessary
- Liaise closely with Research Divisional Lead / Research Specialty Lead
General responsibilities:
- Assist with the submissions of studies to the required review bodies
- Respond to correspondence to obtain approval, and report all changes and unanticipated problems involving patient care
- Assemble, complete and maintain the required regulatory documentation
- Arrange and attend study meetings
- Take blood/urine/biopsy samples as required by the study protocol
- Centrifuge blood samples as required, separating the whole cells from the serum or plasma where requested
- Store samples at the correct temperature and ship samples to central laboratories as required by study protocol
- Ensure that follow up visits for participants are conducted according to study requirements
- Support the department and organisation by carrying out any other duties that reasonably fit within the broad scope of a job of this grade and type of work
Person Specification:
- Education and Qualification:
- Essential: Degree/ Diploma
- Desirable: Registered Nurse or Registered Clinical Research Practitioner
- Registered Health Professional:
- Essential: Diploma, BSc or equivalent
- Desirable: Good Clinical Practice Certificate
- Able to work as an autonomous practitioner:
- Essential: At least 1 year experience
- Desirable: Involvement in Research studies, directly or indirectly
This post is subject to the Rehabilitation of Offenders Act (Exceptions Order) 1975 and as such it will be necessary for a submission for Disclosure to be made to the Disclosure and Barring Service (formerly known as CRB) to check for any previous criminal convictions. Applicants must have current UK professional registration.
Clinical Research Nurse/Practioner in Chertsey employer: Meeveem Limited
Meeveem Limited is an exceptional employer that values its employees by fostering a collaborative and innovative work culture in the heart of Yorkshire. With a strong focus on professional development, employees are encouraged to grow their skills and advance their careers while enjoying competitive benefits and a supportive environment that prioritises work-life balance. Joining Meeveem means being part of a dynamic team dedicated to making a meaningful impact in the cardiovascular and endovascular sectors.
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