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Clinical Trial Assistant

M42 Health

Abu Dhabi, United Arab Emirates · Full Time

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Experience
Any
Salary
Openings
1
Posted
3 hours ago
Work mode
In office
Education
Bachelor’s degree in Life Sciences or related field
Eligibility
UAE National (Emirati) candidates with a Bachelor’s degree in Life Sciences or a related field are eligible to apply.
Resume
Required to apply

Where you'll work

Job description

Overview

M42 Health is a global healthcare leader using artificial intelligence, advanced technology, and genomics to drive new approaches in health for people and the planet. Based in Abu Dhabi, the organization combines specialist facilities with integrated solutions such as genomics and biobanks to support precise, preventive, and predictive care at scale.

Insights Research Organization & Solutions (IROS) is the United Arab Emirates’ first locally founded contract research organization. It focuses on accelerating healthcare research through high-quality clinical trials, data-led solutions, and regulatory support that help advance drug and therapy development and strengthen the region’s contribution to global healthcare innovation.

In this role, you will support the Clinical Operations team by helping ensure that clinical trials are run efficiently and properly documented. The position involves maintaining trial master files and investigator site files, assisting with trial supplies, and supporting adherence to Good Clinical Practice standards. After appropriate training, you may also assist Clinical Research Associates during site visits.

Responsibilities

  • Support day-to-day administrative and operational tasks for clinical study activities.
  • Organize, assess, and store study records in accordance with Good Clinical Practice requirements.
  • Help manage document tracking, trial supplies, and audit preparation for study files.
  • Maintain compliance with standard operating procedures, regulatory expectations, and data quality standards.
  • Work closely with internal colleagues and external partners to keep study activities on track.

Requirements

  • Bachelor’s degree in Life Sciences or a closely related discipline.
  • Basic knowledge of clinical research workflows and the stages of clinical trials.
  • Strong skills in organization, communication, and handling multiple priorities.
  • Comfort using MS Office and document management tools.
  • Familiarity with Good Clinical Practice; certification is an advantage.
  • UAE National (Emirati), as part of the organization’s national development commitment.

Additional Information

This position is based in Abu Dhabi, Abu Dhabi Emirate, United Arab Emirates and is offered as a full-time onsite role.

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