Clinical Research Nurse Critical Care and Anaesthesia

Post Date : 13-Mar-2026 Close Date : 25-Mar-2026 Job Title : Clinical Research Nurse Critical Care and Anaesthesia Department : Anaesthesia Reporting to : Prof Ger Curley, Head of Department of Anaesthesia (and/or nominee) Location : Clinical Research Centre, Beaumont Hospital Contract/Duration : Specified purpose contract for 1 year with possibility for renewal Remuneration : CNM 1, INMO Salary Scale Closing Date : 9:00am on Wednesday 25th of March Summary of Post This 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 are : Conducting 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 team Ensuring 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 Responsibilities To 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 include : Providing nursing expertise and care to participants participating in a clinical trial Ensuring participants have an understanding of the proposed research and standard treatment options Personal & Professional Development : Participate in training programmes, workshops and continuing education activities relevant to the role Pursue professional certifications and credentials to enhance expertise Maintain professional registration Take responsibility for own professional and competency development Undertake mandatory training in accordance with CRC SOPs and relevant study protocols including ICH-GCP certification Qualifications/Experience – Mandatory : Must be registered with an appropriate division of Nursing and Midwifery Board of Ireland Have successfully completed bachelor’s degree level or above, nursing education Have a minimum of 5 years post registration experience Have a minimum of 3 years ICU experience Have good IT skills including Microsoft Office, email etc. Evidence of organisation and project management skills Excellent communication, organisational and interpersonal skills Understanding of research methodologies, Good Clinical Practice (GCP) guidelines and regulatory requirements Ability to work independently, self directed but also works well within a team and under supervision and direction Knowledge & Experience – Desirable : Previous experience working as a clinical research nurse Certificate in Good Clinical Practice Particular to this position : Some flexibility around working hours will be required in response to the varying demands of the post We are all too aware that imposter syndrome and the confidence gap can sometimes stop fantastic candidates putting themselves forward, so please do submit an application — we’d love to hear from you. Application Process Please apply online through the RCSI careers portal on the closing date with your CV and cover letter. Click here to read our Recruitment and Selection Policy for Researcher. Informal Enquiries : Informal enquiries are invited in the first instance through Susanne Lalor susanneLalor@rcsi.ie. All applications for this post must be made through the career's webpage www.rcsi.com/careers.     Please note that we do not accept CVs directly. Garda vetting and occupational health review may be required for this role, depending on the nature of the duties and responsibilities. Further information will be provided during the recruitment process. Eligibility to Work in Ireland Visa sponsorship is available for candidates who fully meet the essential criteria of the role. Candidates who require a work permit or hosting agreement are welcome to apply. Proof of eligibility documentation will be required at a later stage in the recruitment process. Please note that sponsorship is subject to approval by the relevant Irish authorities and role-specific eligibility. Click on the link(s) below to view documents Filesize JD_CRN Critical Care 509.9 Return to Search Apply for Job