Overview
The post holder will undertake screening and recruitment of research participants for the PROSPECT study and other BRC-funded studies, provide support and information to participants, organise follow up (including interviews), and record research data accurately and promptly. The role includes embedding a culture of research participation within clinical areas, collaborating with clinical staff to integrate research activities into routine care, and acting as a liaison between clinical and research teams to facilitate Good Clinical Practice (GCP). The post holder will report problems and identify solutions and contribute to the conduct and reporting of systematic reviews and qualitative research, as well as to the dissemination of findings through papers and conferences.
Responsibilities
* Screen and recruit research participants for the PROSPECT study and other BRC-funded studies.
* Provide participants with information and support related to the research study.
* Organise follow up for research participants, including conducting interviews as required.
* Record research data and documentation accurately and in a timely manner.
* Embed a culture of research participation in clinical areas and work with clinical staff to integrate research activity into routine clinical care.
* Act as a liaison between clinical and research teams to facilitate Good Clinical Practice.
* Report problems and issues with the research study to the appropriate person in a timely manner and identify solutions.
* Conduct and report systematic reviews.
* Conduct and analyse qualitative research.
* Prepare papers for peer‑reviewed journals and present research results at conferences.
* Attend local and national meetings to acquire training for specific research activities as required.
* Maintain awareness of current relevant treatments and advances and use this knowledge to maintain high standards of evidence‑based care for patients related to the research activity.
* Access medical records for research purposes where appropriate and conduct literature searches to inform the study.
* With support, conduct qualitative interviews and analyse qualitative data; with support, write papers reporting study results for peer‑reviewed journals.
* Undergo required training including Good Clinical Practice (GCP), GDPR data collection techniques and analysis.
Clinical Responsibility
* Provide patients/family members with comprehensive information in an easily understandable way to facilitate informed consent and consultee opinion, including the use of translation and interpretation services as required.
* Ensure all patients are informed about standard care and the research activity, including structure, potential risks, benefits and side effects.
* Be sensitive to the emotional needs of patients and relatives, using tact and judgement regarding research participation.
* Provide support and advice to patients, relatives and staff before, during and after research activity.
* Ensure voluntary participation and the right to refuse or withdraw at any point.
* Act as a patient advocate and coordinate study procedures to maximise patient comfort and wellbeing.
* Collect data from medical records and complete Case Report Forms (CRFs) as required.
* Work within the multi-disciplinary team to promote individualised care for patients.
* Maintain a confidential register of patients willing to be contacted about future research studies.
* Ensure study team members meet requirements in accordance with the research protocol and Good Clinical Practice.
* Assist with administration of the study and storage of relevant documents.
* Prepare reports for funders, papers for publication and present findings at meetings and conferences.
Leadership and management
* Liaise with designated staff within departments to ensure the smooth running of the research study.
* Record and report any serious adverse events to the appropriate authorities.
* Lead the interviewing arm of the study, including conducting qualitative interviews, processing complex data, and formulating follow-up questions and analyses.
* Follow standard operating procedures to signpost interview participants to support if they become upset or distressed during interviews.
* Work at all times under regulations described in ICH, Good Clinical Practice (GCP) and current research governance regulations.
* Liaise with external investigators as necessary and with R&D staff as appropriate.
* Present findings at meetings and conferences and liaise with PPI representatives.
Person specification
* Honours degree in Nursing or a related health subject.
* UK professional registration at Grade 6 or equivalent.
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