Job DescriptionJob Title ; Clinical Trials NurseJob Description: Clinical Trials NuThe Clinical Trials Nurse (CTN) plays a key role in the delivery of clinical research by providing nursing expertise and direct patient care within clinical trial settings. The CTN ensures participant safety, supports study procedures, and promotes high-quality data collection in compliance with study protocols, Good Clinical Practice (GCP), and regulatory requirements. This role works closely with investigators, research coordinators, and multidisciplinary teams to ensure efficient and ethical conduct of clinical studies.Provide nursing care to clinical trial participants, including screening, consenting, administering treatments, monitoring, and follow-up.Educate participants and their families about study procedures, potential risks, and benefits.Ensure accurate and timely documentation of trial-related procedures, interventions, and outcomes.Support principal investigators and research teams in implementing study protocols.As required administer investigational products (oral, IV, injection, etc.) safely and in accordance with protocol and nursing standards.Monitor participants for adverse events, report findings promptly, and contribute to safety management.Maintain compliance with ICH-GCP, research ethics, and institutional policies.Participate in site initiation, monitoring visits, audits, and inspections as required.Assist with trial logistics such as scheduling, data entry, sample handling, and record keeping.Act as a liaison between participants, clinical teams, and study sponsors/CROs.Participate and support research dissemination activitiesExperience in clinical research, clinical trials, or relevant specialty nursing.Strong understanding of research ethics, ICH-GCP guidelines, and regulatory frameworks.Excellent communication, patient care, and organizational skills.Ability to work independently and as part of a multidisciplinary team.Competency in electronic health records (EHR), clinical trial management systems (CTMS), and Microsoft Office.Person SpecificationQualificationsEDUCATION:· Degree in Nursing (Required)· Post graduate qualification in Research methodology desirableExperience(Amount and Type)· Substantial experience of working in an acute hospital at a senior level.· Minimum 3 years' experience in Acute Medical Oncology· Experience in phlebotomy, IV insertion and administration of investigational products.· Familiarity with informed consent process· Familiarity with adverse event reporting and pharmacovigilance processes· Knowledge of sample management and chain of custody· Experience of collating and reporting complex dataJob Specific Competencies and Knowledge· Ability to read, analyse and interpret research study protocols, agreement documents and patient education materials.· Ability to write research activity reports and summaries to support dissemination activities.· Knowledge of Good Clinical Practice (CGP), Data Protection (GDPR) requirements· Knowledge of accreditation requirements (Joint Commission, HIQA, ASCO)Personal Competencies· All posts in Beacon Hospital require a high level of flexibility to ensure the delivery of an effective and efficient service. Therefore, the post holder will be required to demonstrate flexibility as and when required by their manager and / or hospital management.· Professional and positive approach in building relationships and quickly gain credibility with work colleagues.· Self-motivated, dynamic, creative and able to work on own initiative.Apply for this positionJob Types: Full-time, PermanentPay: €31,026.06-€119,852.91 per yearBenefits:On-site parkingSick pay