ID
2025-4551
Category
Research
Asset : Name
IROS
City
Abu Dhabi
Overview
IROS is a leading Contract Research Organisation (CRO) in the Middle East, specializing in clinical trials across diverse therapeutic areas and integrating real-world data. We are seeking a highly qualified Clinical Research Associate (CRA) to join our team and play a key role in advancing clinical research excellence.
About the Role
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: 4–6 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.
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