Clinical Training Research Nurse

Overview

Responsibilities

• Coordinate and support assigned clinical research studies in collaboration with Principal Investigators and multidisciplinary teams.
• Supportpatient recruitment, screening, informed consent, sample collection, and data documentation in accordance with study protocols and ethical standards.
• Ensure thesmooth day-to-day delivery of research activities, maintaining data integrity, quality, and regulatory compliance.
• Develop, deliver, and maintainclinical training programmes for research nurses and clinical staff, including study protocols, GCP, and regulatory requirements.
• Providementorship, coaching, and ongoing education to new and existing research staff, ensuring consistent standards of practice.
• Maintain accuratetraining records, competency assessments, and documentation.
• Act as a key point of contact forpatient, site, and study-related queries, providing professional and compassionate communication.
• Collaborate closely with internal departments and external stakeholders to support research operations and outreach activities.
• Prepare for and supportinternal and external audits, inspections, and regulatory reviews.
• Ensure adherence to all organisational policies, regulatory requirements, and professional standards.
• Identify and manage risks, contributing to a culture ofcontinuous improvement and operational excellence.
• Promoteperson-centred care, building trust and positive relationships with participants, staff, and stakeholders.

Qualifications

• Bachelor’s degree or diploma in Nursing.
• Valid DOH Nursing License (mandatory for this patient-facing role).
• Experience in clinical nursing, with exposure to clinical training, education, or mentoring.
• Phlebotomy and sample collection experience including blood, urine, saliva, swab and faecal specimens.
• Previous experience in clinical research or clinical trials is desirable but not essential.
• Understanding of Good Clinical Practice (GCP) and clinical research standards (e.g. ICH-GCP, FDA, EMA) is preferred.
• Experience supporting audits, inspections, or regulatory submissions (e.g. DoH IRB) is an advantage.
• Strong written and verbal communication skills, with the ability to train and mentor clinical staff.
• Excellent organisational skills with a high level of attention to detail.
• Ability to manage multiple priorities and work effectively both independently and within multidisciplinary teams.
• Proficiency in Microsoft Office and familiarity with research systems and databases.
• Compassionate, patient-centred approach with a commitment to high-quality care and research excellence.