Clinical Trial Assistant
M42 Health
Date: 2 weeks ago
City: Remote
Contract type: Full time
Remote
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.
Insights Research Organization & Solutions (IROS) is the UAE’s first homegrown Contract Research Organization (CRO) dedicated to advancing healthcare research. By delivering world-class clinical trials, data-driven solutions, and regulatory expertise, IROS empowers innovation, accelerates drug and therapy development, and strengthens the region’s role in shaping the future of global healthcare.
As a Clinical Trial Assistant, you will play a key support role within the Clinical Operations team, ensuring efficient execution and documentation of clinical trials. This includes maintaining trial master files (TMF), investigator site files (ISF), assisting with trial supplies, and ensuring compliance with Good Clinical Practice (GCP) standards. You will also support Clinical Research Associates (CRAs) and may participate in site visits following training.
Responsibilities
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.
Insights Research Organization & Solutions (IROS) is the UAE’s first homegrown Contract Research Organization (CRO) dedicated to advancing healthcare research. By delivering world-class clinical trials, data-driven solutions, and regulatory expertise, IROS empowers innovation, accelerates drug and therapy development, and strengthens the region’s role in shaping the future of global healthcare.
As a Clinical Trial Assistant, you will play a key support role within the Clinical Operations team, ensuring efficient execution and documentation of clinical trials. This includes maintaining trial master files (TMF), investigator site files (ISF), assisting with trial supplies, and ensuring compliance with Good Clinical Practice (GCP) standards. You will also support Clinical Research Associates (CRAs) and may participate in site visits following training.
Responsibilities
- Provide administrative and operational support to clinical projects.
- Manage, review, and archive study documentation in line with GCP.
- Assist in document control, trial material handling, and file audits.
- Uphold data integrity and compliance with SOPs and regulatory guidelines.
- Collaborate effectively with internal teams and external stakeholders.
- Bachelor’s degree in Life Sciences or related field.
- Understanding of clinical research processes and trial phases.
- Strong organizational, communication, and multitasking skills.
- Proficiency in MS Office and document management systems.
- Knowledge of GCP (certification preferred).
- UAE National (Emirati) - as part of IROS’ commitment to national development.
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