Overview
IROS is the first UAE-based Contract Research Organization (CRO), specializing in healthcare research and committed to the highest scientific and ethical standards. A proud member of the M42 network, Abu Dhabi’s leading HealthTech ecosystem backed by Mubadala and G42, IROS delivers clinical trial management and real-world data integration services across all therapeutic areas.
As a Clinical Trial Assistant, you will play a vital support role in the Clinical Operations team, contributing to the 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
- Support the clinical operations team in daily project coordination and trial administration.
- Maintain and organize essential documents in Trial Master Files (TMF) and Investigator Site Files (ISF).
- Assist in the handling, tracking, and shipment of trial supplies and study materials.
- Participate in internal quality checks, file audits, and compliance monitoring.
- Ensure all documentation aligns with ICH-GCP, SOPs, and regulatory requirements.
- Collaborate closely with Clinical Research Associates (CRAs) and other cross-functional stakeholders.
- May attend site visits and assist in monitoring activities after appropriate training.
Qualifications
- 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).
- Emirati Talent – as part of IROS’ commitment to national development.
