Description

Job Description

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 Research Associate, you will be responsible for supporting clinical trial operations from study start-up through to close-out. You will collaborate with study sites, sponsors, and internal teams to ensure compliance, data integrity, and adherence to international standards of Good Clinical Practice (GCP).

Responsibilities

• Conduct feasibility studies and site qualification assessments.
• Support study setup, including regulatory submissions and documentation.
• Manage regulatory compliance and maintain essential study records.
• Perform monitoring visits, review protocol deviations, and report adverse events.
• Ensure data integrity and adherence to GCP.
• Provide timely updates to clients and internal stakeholders.
• Oversee study site closure and final documentation.
  

Qualifications

• Education: Bachelor’s degree in Life Sciences.
• Experience: 3-4 years in clinical research, with direct involvement in at least five interventional clinical trials.
• Skills & Knowledge:
• Strong organizational, decision-making, and time management skills.
• Excellent communication and collaboration abilities, particularly in cross-cultural environments.
• Proficiency in Microsoft Office applications.
• Certification in Good Clinical Practice (GCP).
• Demonstrated ability to lead, document thoroughly, and work effectively in a matrixed structure.