Ireland

Clinical Trials Nurse, Sandyford

Clinical Trials Nurse, Sandyford
Description
Job Description

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.





Requirements
  • 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.


Benefits

  • Fully Funded Private Health Insurance
  • Generous Salaries
  • Educational Support
  • Excellent Career Opportunities
  • Income Protection
  • Subsidised Parking
  • Maternity Leave



Requirements
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.
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