IROS CRO, a leading Contract Research Organisation in the Middle East, is seeking a Clinical Research Associate (CRA) to support clinical trial operations across diverse therapeutic areas. The role is full-time and on-site in Abu Dhabi, involving study start-up, monitoring, compliance, and collaboration with study sites and sponsors.

Key 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 Good Clinical Practice (GCP).

• Provide timely updates to clients and internal stakeholders.

• Oversee study site closure and final documentation.

Requirements / Qualifications:

• Bachelor’s degree in Life Sciences.

• 4–6 years of clinical research experience, with direct involvement in at least five interventional clinical trials.

• Strong organizational, decision-making, and time management skills.

• Excellent communication and collaboration abilities, especially in cross-cultural environments.

• Proficiency in Microsoft Office applications.

• Certification in Good Clinical Practice (GCP).

• Ability to lead, document thoroughly, and work effectively in a matrixed structure.

Salary & Benefits:

• Competitive salary (details to be shared during the interview).

• Opportunity to work with a global, AI-powered healthcare organization.

• Exposure to advanced clinical research methodologies and international standards.