Job Title: Clinical Research Nurse Critical Care and AnaesthesiaReporting to: Prof Ger Curley, Head of Department of Anaesthesia (and/or nominee)Location: Clinical Research Centre, Beaumont HospitalContract/Duration: Specified purpose contract for 1 year with possibility for renewalRemuneration: CNM 1, INMO Salary ScaleClosing Date: 23:45 on the 12th of AprilSummary of PostThis is an exceptional opportunity for a senior nurse with passion, vision and energy to be a part of the research team in the Dept of Anaesthesia and Critical Care. We are seeking a motivated, flexible candidate with a robust clinical skill set to work as a Clinical Research nurse in the dynamic environment of Critical Care. This position offers an exciting opportunity to contribute to cutting‑edge research in the field of critical care medicine. The successful candidate will play a pivotal role in advancing our understanding of critical care treatments and improving patient outcomes. The research nurse will support research trials based at the Intensive Care Unit at Beaumont Hospital. As part of this role research projects will range from investigator lead studies to clinical trials involving investigational medicinal products specifically related to Critical Care and Anaesthesia. The Clinical Research Nurse will play a vital role in the implementation, and coordination of clinical research studies.Specifically, the duties of the post areConducting research activities including screening, consenting and recruiting patients for clinical trials. Administering study interventions and collecting data in an accurate and timely fashion according to research protocols.Working with an interdisciplinary team to ensure effective coordination and execution of research.Maintaining research compliance by adhering to ethical guidelines, research regulations and institutional policies with a high standard of record keeping.Educating and support patients and members of the research teamEnsuring continuous professional development to facilitate up to date knowledge on research developments, advances in critical care and emerging technologies and to enhance knowledge and skills.Principal Duties and ResponsibilitiesTo work to the RCSI CRC’s standard operating procedures for clinical trials and academic research.Be responsible for the coordination of studies, to include but not limited to: Screening and recruitment of study participants, performing study procedures, data collection, coordination of study visits and follow up and safety reporting.Play an active role in driving and promoting clinical research projects in the ICU department.Assist the Principal Investigator in delivering study training to ICU staff, including new research team members.To ensure patient confidentiality and dignity is assured and maintained at all times during a clinical trial/research project.Responsible for the maintenance and upkeep of clinical research governance documentation.Ensure that all hospital and RCSI governance procedures and approvals have been adhered to and are in place prior to the commencement of all research projects.Prepare for Internal / Sponsor / HPRA audits as required.Liaise with patients and their relatives (if appropriate) to inform them on the proposed research and standard treatment options.Work with the Principal Investigator and the ICU staff in the conduct of the study in line with International Conference on Harmonization Good Clinical Practice Guidelines and the applicable regulations.Some reasonable flexibility around working hours will be required in response to the varying demands of the post.To carry out other duties as appropriate to the post as may be assigned from time to time by the Principle Investigator, appointee, CRC Director or CRC Director of Nursing.Clinical Practice Responsibilities will includeProviding nursing expertise and care to participants participating in a clinical trialEnsuring participants have an understanding of the proposed research and standard treatment optionsPersonal & Professional DevelopmentParticipate in training programmes, workshops and continuing education activities relevant to the rolePursue professional certifications and credentials to enhance expertiseMaintain professional registrationTake responsibility for own professional and competency developmentUndertake mandatory training in accordance with CRC SOPs and relevant study protocols including ICH-GCP certificationQualifications/Experience – MandatoryMust be registered with an appropriate division of Nursing and Midwifery Board of IrelandHave successfully completed bachelor’s degree level or above, nursing educationHave a minimum of 5 years post registration experienceHave a minimum of 3 years ICU experienceEvidence of organisation and project management skillsExcellent communication, organisational and interpersonal skillsUnderstanding of research methodologies, Good Clinical Practice (GCP) guidelines and regulatory requirementsAbility to work independently, self directed but also works well within a team and under supervision and directionPrevious experience working as a clinical research nurseCertificate in Good Clinical PracticeParticular to this positionSome flexibility around working hours will be required in response to the varying demands of the post
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