Lead execution of all approved evidence-generation studies.
Develop detailed implementation plans with clear timelines, milestones, budgets, and forecasts.
Monitor study progress, risks, and mitigation actions throughout execution.
Maintain study master files and ensure complete, compliant, and inspection-ready documentation.
Support study-related audits and inspections as required.
Act as the primary contact for all CRO partners.

🎯 Requirements

Bachelor's degree in Medicine, Pharmacy, Clinical Pharmacy, Life Sciences, Public Health
Minimum 3 years of relevant experience in Clinical Research Operations and/or Evidence Generation.
Demonstrated experience in study start-up, execution, monitoring, close-out, vendor management
Experience as Clinical Research Coordinator (CRC), Clinical Research Associate (CRA), Clinical
Good understanding of clinical research methodologies, real-world evidence studies, ICH-GCP
Fluent in English and Arabic.

🛃 Visa sponsorship

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