| Job Location | Abu Dhabi, United Arab Emirates (UAE) |
| Education | Not Mentioned |
| Salary | Not Mentioned |
| Industry | Medical, Healthcare, Diagnostics |
| Functional Area | Not Mentioned |
Roles & ResponsibilitiesConduct thorough audits of clinical trial data, ensuring accuracy, completeness, and adherence to protocols and regulations, meticulously examining source documents and electronic data capture systems.Verify patient safety and data integrity by assessing adverse event reporting, protocol deviations, and laboratory data, focusing on potential risks and inconsistencies.Evaluate clinical trial sites for compliance with Good Clinical Practice (GCP) guidelines, identifying areas for improvement in site operations and data management processes.Prepare comprehensive audit reports, clearly documenting findings, observations, and recommendations for corrective actions, providing evidence-based insights.Desired Candidate ProfileA Bachelor's degree in a relevant field such as Biology, Pharmacy, or a related healthcare discipline, providing a strong foundation in scientific principles.Demonstrated experience in clinical research or a related field, showcasing a practical understanding of clinical trial processes.Relevant certifications such as Certified Clinical Research Professional (CCRP) or Certified Quality Auditor (CQA), demonstrating commitment to quality and expertise.Minimum of 3-5 years of experience in clinical research, auditing, or a related field, providing a solid understanding of clinical trial methodologies.
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