A clinical research organization in Dubai seeks a Clinical Trial Monitor responsible for overseeing phase I to IV studies. The role involves site visits, managing trial site activities, and ensuring regulatory compliance. A Bachelor's degree in a health-related field and at least two years of monitoring experience are required. Candidates will engage with stakeholders and support compliance with Good Clinical Practice (GCP) standards. This position offers a dynamic work environment in the UAE.

Opportunity to work on phase I to IV clinical studies

Oversee clinical trials from phase I to IV by conducting site visits, managing study activities, and ensuring adherence to regulatory standards. Collaborate with diverse stakeholders and champion Good Clinical Practice (GCP) compliance while working in the vibrant healthcare landscape of Dubai.

Clinical Research Associate II Site Monitoring Pro

Clinical Trial Monitoring

Regulatory Compliance

Good Clinical Practice (GCP)

Site Visit Management

Stakeholder Engagement

Clinical Data Management

Trial Site Coordination

Medical Terminology

Clinical Research Protocols

Risk Management

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Clinical Research Associate II Site Monitoring Pro

Junior Research Scientist in the Center for Brain and Health (CBH) – Dr. Kartik Sreenivasan and Dr. Bas Rokers