- 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. 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 – Essential:
- 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 Knowledge & Experience – Essential:
- Have relevant ICU experience
- Have relevant experience post registration experience in acute hospital setting, ideally 3 years
- Have good IT skills including Microsoft Office, email etc.
- Evidence of organisation and project management skills
- Excellent communication, organisational and interpersonal skills
- Understand of research methodologies, Good Clinical Practice (GCP) guidelines and regulatory requirements Knowledge & Experience – Desirable:
- Previous experience working as a clinical research nurse
- Post graduate experience is a distinct advantage 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.
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Clinical Research Nurse Critical Care and Anaesthesia - Dublin, Ireland - RCSI
Description
Summary of Post
We are seeking a dynamic, flexible with a strong clinical skill set research nurse to support research trials in Department of Anaesthesia and Critical Care. This position will involve working as part of the research team in the Department of Anaesthesia. 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: