Part-Time Clinical Trials Research Nurse

Royal College of Surgeons in Ireland (RCSI)

Dublin

On-site

EUR 25,000 - 42,000

Part time

2 hours ago
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Job summary

Royal College of Surgeons in Ireland (RCSI) seeks a part-time clinical research nurse (0.5 FTE) to support trial activities at Connolly Hospital. The role demands nursing registration with NMBI, strong clinical skills, and experience in clinical research or trials.

You will recruit, follow up, coordinate visits, and ensure high-quality data and compliance. The position is for a one-year specified purpose contract, offering a collaborative environment with opportunities for professional

Qualifications

  • Must be on the live nursing register with NMBI.
  • Degree level nursing education or equivalent.
  • Experience in clinical research or trials preferred.
  • Excellent communication and organisational skills.
  • Proficiency with MS Office.

Responsibilities

  • Work within SOPs and ICH-GCP/HPRA protocols for clinical research activities.
  • Support ongoing clinical research projects through recruitment, follow-ups, and coordination.
  • Ensure proper documentation, data entry, and regulatory submissions for trials.
  • Maintain participant confidentiality and accurate study records.
  • Coordinate study visits, timelines, and monitoring activities.
  • Prepare reports and assist in audits and regulatory reviews.
  • Attend study-related meetings and contribute to protocol feasibility.
  • Operate the department's blood pressure monitoring service as required.

Skills

Excellent communication skills
Teamwork and collaboration
Analytical/problem solving
Flexibility/adaptability
IT skills (MS Office)

Education

NMBI nursing registration
Nursing degree (RCSI level 9 module eligible)

Tools

MS Office

Job description

Royal College of Surgeons in Ireland (RCSI) seeks a part-time clinical research nurse (0.5 FTE) to support trial activities at Connolly Hospital. The role demands nursing registration with NMBI, strong clinical skills, and experience in clinical research or trials.

You will recruit, follow up, coordinate visits, and ensure high-quality data and compliance. The position is for a one-year specified purpose contract, offering a collaborative environment with opportunities for professional

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