Senior Research Officer

In addition to the below summary you need to familiarize yourself with full Job Description and Person Specification documents attached to this advert. Research and Communication Administer, co-ordinate and manage the collection of data relating to ongoing clinical studies in the portfolio. Screen, identify, recruit and follow-up appropriate patients for clinical studies. Demonstrate excellence and professionalism in all modes of communication: in writing, in person, via telephone and using new media. Carry out and/or monitor all trial-related and other research clinical care procedures for research participants to the highest safety standards. Demonstrate keyboard, word processing and database skills, adapting to the required needs of specialist and trial-specific systems. Perform trial and other research procedures competently and in accordance with local Trust policies e.g. ECG, sample processing, pregnancy testing, venepuncture, I.V cannulation. Ensure that the processing and storage of biological samples meets the necessary requirements of the research protocol in order to ensure safe handling and quality. Take responsibility for seeking consent from patients and relatives and/or provide support to medical colleagues in doing so. Approach patients and/or relatives during their inpatient stay to gain retrospective informed consent where appropriate. Liaise with clinical research associates involved in specific clinical trials and report any concerns or safety problems to the appropriate authority. Undertake research work competently under minimal supervision. Maintain accurate records and other documentation appropriate to the individual trials. Take responsibility for groups of research patients in specific trials to coordinate all aspects of their participation. Contribute to the efficient set-up of new clinical trials as required and take the role of lead on individual trials to improve continuity and effectiveness. Ensure all trials are carried out in accordance with ICH-GCP guidelines. Represent at investigator meetings and research conferences associated with clinical trials and as an advocate for NHS research and evidence-based care. Ensure G.P.s are informed of, and updated on their patients participation in clinical trials in the portfolio where required. Ensure that the rights, dignity and confidentiality of research participants and their families are protected at all times. Actively maintain and promote effective communication within the department, the multi-professional team, patients and their families and other departments or organisations within the trust and network. Be a committed and supportive member of the research team. Take responsibility for ensuring safe keeping and archiving of all data from clinical studies in line with relevant legislation and local guidance. Prepare for and facilitate trial monitoring by sponsors and regulatory authorities as required. Assist in audit inspections and demonstrate knowledge of the audit process as a resource for clinical colleagues. Education Ensure all members of the multi-professional team are aware of the clinical trials through formal and informal teaching. Keep abreast of developments in clinical trials research in order to carry out the role effectively and competently. Adopt a proactive approach to ensuring your own education and demonstrate a commitment to the development of the skills, knowledge and confidence of colleagues. Assist in the induction and education of all members of the multi-professional team in the research process, details of specific trials and act as a general resource on research matters when required. Practice Adopt a professional and patient-centred approach to prioritising workload and demonstrate effective strategies for managing the care of research patients and their families. Demonstrate excellence in carrying out research procedures and techniques in accordance with agreed policies and standards when applicable. Report to medical and/or senior relevant staff on the condition and progress of patients. Demonstrate excellence in carrying out trial-specific procedures / techniques in accordance with trial protocols and standard operating procedures. Work in a supernumerary capacity for occasional clinical shifts if required to maintain clinical skills and links with clinical areas. Contribute towards maintaining an environment conducive to learning and development. Contribute towards ensuring that research influences practice and education. 4. Professional Maintain a proactive attitude to patient safety and ensure the prevention of harm to yourself, your patients and your colleagues including the timely and independent use of trial, research and all standard local safety reporting systems. Identify personal objectives, reflect on progress and formally revise a personal development plan annually, in order to enhance their contribution to the department using the Performance Development Review (PDR) process. Following individual performance management, liaise with the clinical and research leads in agreeing how identified training and development needs are to be met. Ensure that your own practice is kept updated, using an acceptable model of clinical supervision. Take every opportunity to expand your practice and knowledge in line with the principles contained with your relevant professional registration. Represent the Research & Innovation research teams across and beyond NUH by displaying exemplary standards of behaviour and professionalism. Ensure that the elements contained within your relevant professional registration) are adhered to by yourself and others, in particular those relating to professional accountability. Contribute to meeting the Directorate and Trust Strategic Objectives, Targets & Annual Plans for research delivery.