Clinical Research Nurse x2

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My client delivers a wide range of projects and programmes of work; from large clinical trials to EHR data enabled pragmatic clinical trials as well as feasibility studies utilising routinely collected healthcare data. They work primarily with pharmaceutical and NHS-related clients and are the market-leader in providing these services. They are looking for 2 fixed-term clinical research nurses to join their team.Job Purpose: As a Research Nurse, you will provide specialist skills and knowledge to support the delivery of clinical research studies. You will liaise with clinical investigators and sponsor companies to manage trial protocols and ensure high quality research with a commitment to participant safety and welfare. The nature of the work is unpredictable, and you will be expected to be flexible and responsive in order to manage various aspects of the job at short notice. You will be expected to participate fully in your own personal development.MAIN DUTIES AND RESPONSIBILITIES ResearchEnsure that all research is delivered in accordance with ICH GCP guidelinesEnsure familiarity with risk issues pertaining to confidentiality of participant and research related documentation (General Data Protection Regulation 2018 and Caldicott Review 2013)Ensure compliance with all study protocolsResponsible for managing multiple sites from set up to closure. To include identification and recruitment of patients in accordance with study protocols and to agreed targets and timelinesResponsibility for participant screening, eligibility assessment, and provision of information to facilitate effective informed consent or assentResponsible for recording, reporting and escalating adverse drug reactions and adverse events, according to study protocol and Clinical Trial RegulationsResponsible for the processing and shipment of biological samplesCollaborating with any investigations and subsequent managementContribute to research governance processes including critical incident reporting in line with standard operating procedures (SOPs)Ensure clear and accurate records and documentation to support and record all research activity using databases, software and electronic health care records as requiredWork collaboratively with data managers and clinical research monitors to ensure timely resolution of data queriesParticipate in audits and inspections as requiredSupport and execute all activities in line with ISO standards where relevant (ISO 9001:2015)Effective management of resourcesWork in a variety of settings including hospital, community settings, possibly as a lone-worker, to meet the demands of studiesEssential skills: Qualifications Registered Nurse NMC Level 1Experience and SkillsEffective communication and interpersonal skillsExperience of explaining complex concepts to patients in a clear and simplified mannerEvidence of continuous professional developmentAble to work autonomously and as a team playerVenepunctureMeticulous attention to detail and high level of accuracyDemonstrable IT skillsFlexible workingHighly motivated with the ability to organise own work and meet deadlinesClean driving licenceWilling to use own car (mileage recompensed following policy) and insure car for business useKnowledge Research knowledge of regulations and governance in clinical research including EU directives and ICH GCP requirements Desirable skills: Qualifications 1st level degree or studying towardsExperience and Skills Experience working in Primary CareIV therapy cannulationPresentation skills To find out more about Real please visit www.realstaffing.comReal Staffing, a trading division of SThree Partnership LLP is acting as an Employment Business in relation to this vacancy| Registered office | 1st Floor, 75 King William Street, London, EC4N 7BE, United Kingdom | Partnership Number | OC387148 England and Wales