Experienced Clinical Research Associate - Multi Sponsored

About the role

We are looking for an Experienced Clinical Research Associate to support multi‑sponsored studies in Dubai. The role involves on‑site monitoring, ensuring compliance with protocols, regulations and sponsor expectations.

Key responsibilities

• Conduct site selection, initiation, monitoring and close‑out visits in line with GCP and ICH guidelines.
• Drive and track subject recruitment plans with sites to meet project timelines.
• Provide protocol and study training to site staff and maintain regular communication.
• Assess site practices for quality and regulatory compliance, escalating issues when needed.
• Track regulatory submissions, enrollment, CRF completion, data queries and study progress.
• Maintain Trial Master File and Investigator Site File according to local requirements.
• Document visit findings, generate reports and follow‑up letters.
• Collaborate with internal study team and support site financial management and invoice processing.

Required profile

• Bachelor’s degree in a scientific discipline or healthcare (preferred) or equivalent experience.
• Minimum 1 year of on‑site monitoring experience in clinical trials.
• Strong understanding of clinical research regulations, GCP and ICH guidelines.
• Good therapeutic and protocol knowledge as provided by company training.

Required skills

• Good Clinical Practice (GCP) knowledge.
• International Conference on Harmonization (ICH) guideline expertise.

What we offer

• Opportunity to work with a leading global health data company.
• Exposure to multi‑sponsored clinical studies across therapeutic areas.