RecruitNet International Ltd specialises in healthcare recruitment for both domestic and overseas candidates across Hospitals, Nursing Homes, Home Care, and Community Care settings.
We are currently hiring a Clinical Trials Nurse for a leading hospital in Dublin, Ireland.
Working Hours: 37 hours per week.
Key Responsibilities
Provide high‑quality nursing care to clinical trial participants, including screening, consenting, administering treatments, monitoring, and follow‑up.
Educate participants and their families on study procedures, potential risks, and benefits.
Ensure accurate and timely documentation of all trial‑related procedures, interventions, and outcomes.
Support Principal Investigators and research teams in implementing study protocols.
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 guidelines, research ethics, and institutional policies.
Participate in site initiation, monitoring visits, audits, and inspections as required.
Assist with trial logistics including scheduling, data entry, sample handling, and record keeping.
Act as a liaison between participants, clinical teams, and study sponsors/CROs.
Support research dissemination activities as needed.
Assist the clinical team with daily study operations.
Communicate with internal and external customers to increase project and departmental efficiencies.
Coordinate scheduling of internal team meetings, cooperate with drafted agendas and create meeting minutes; may present during meetings.
Coordinate logistics of study‑related meetings including medical expert meetings, investigator meetings, and kick‑off meetings; assist in project travel plans, reservations, and expense reports.
Maintain project‑related trackers and provide the information to the rest of the study team as needed.
Maintain and use the clinical trial management system (CTMS), create studies within the system per SOPs, track study data, and generate reports.
Assist in the preparation, creation, and quality review of key clinical study documents such as informed consent documents, essential regulatory documents, study manuals, investigator brochures, protocols, clinical study reports, and in the review of investigational product release documents.
Assist in the distribution of key clinical study documents such as investigator brochures, protocols, informed consents, and regulatory submissions.
Follow up on study progress, coordinate updates and retrieval of appropriate regulatory documents throughout the study.
Submit and track essential documents to the Trial Master File (TMF) on an ongoing basis.
Assist in the archival of CRO study files and coordinate the set‑up, filing, maintenance, and periodic review of TMF and project electronic filing systems throughout the study.
Collaborate with other departments and vendors on the review and maintenance of the TMF.
Perform filing, maintenance, and periodic review of project TMF throughout the study, if the task is not delegated to a vendor.
Qualifications
Strong understanding of research ethics, ICH‑GCP guidelines, regulatory frameworks, and data protection requirements (GDPR).
Degree in Nursing (required); postgraduate qualification in Research Methodology desirable.
Substantial senior‑level experience in an acute hospital setting.
Minimum 3 years’ experience in Acute Medical Oncology.
Proficiency in phlebotomy, IV insertion, and administration of investigational products.
Familiarity with informed consent processes, adverse event reporting, and pharmacovigilance.
Knowledge of sample management procedures and chain of custody requirements.
Experience in collecting, analysing, and reporting complex clinical and research data.
Strong communication, patient care, organisational skills, and ability to work independently and within multidisciplinary teams.
Associate’s degree in a life science field preferred.
Minimum 2 years of experience as a clinical trial associate.
Desirable: 4 years of experience as a clinical trial associate and relevant experience in clinical research.
Benefits
Fully funded private health insurance.
Generous salaries.
Educational support.
Excellent career opportunities.
Income protection.
Subsidised parking.
Maternity leave.
Highly competitive salary.
Group pension scheme (company matches contribution rates).
Private medical insurance for the employee.
Ongoing opportunities for career development.
Succession planning and internal promotions.
Education allowance.
Wellness activities.
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