Clinical Training Research Nurse

Abu Dhabi Biobank


Date: 2 weeks ago
City: Abu Dhabi
Contract type: Full time
Overview

M42 is a global health champion powered by artificial intelligence (AI), technology and genomics to advance innovation in health for people and the planet. Headquartered in Abu Dhabi, M42 combines its specialized, state-of-the-art facilities with integrated health solutions like genomics and biobanks, and harnesses advanced technologies to deliver precise, preventive and predictive care, to disrupt traditional healthcare models and positively impact lives globally.

Abu Dhabi BioBank is a state-of-the-art biobanking facility at the forefront of medical research and innovation in the region. By collecting, storing, and analyzing high-quality biological samples, it enables groundbreaking discoveries in genomics, precision medicine, and drug development. As part of M42’s Integrated Health Solutions platform, Abu Dhabi BioBank plays a vital role in advancing population health, accelerating scientific breakthroughs, and addressing global health challenges.

We are seeking a dedicated and highly motivated Clinical Training Research Nurse to join our dynamic Biobank team. This role combines clinical nursing expertise, research coordination, and adult education, and plays a key role in supporting, training, and developing clinical staff involved in research activities.

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.

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