Specialist- Medica Research Section

<div><h3>Job Description</h3><ul><li>Develop, review, and update research policies, guidelines, standards, and procedures in alignment with organizational and regulatory requirements.</li><li>Analyze internal and external research audit reports to identify gaps, risks, and areas for improvement in research governance and compliance.</li><li>Prepare detailed audit summary reports, including findings, root cause analysis, and actionable recommendations.</li><li>Design, implement, and monitor Quality Improvement Plans (QIPs) to address audit findings and enhance research processes and regulatory compliance.</li><li>Track progress of QIPs and ensure timely implementation of corrective and preventive actions (CAPA).</li><li>Support the enhancement of research regulatory frameworks and contribute to strengthening institutional research governance.</li><li>Conduct periodic reviews of research practices and processes to ensure adherence to approved policies and standards.</li><li>Collaborate with internal stakeholders to ensure effective implementation of research policies and audit recommendations.</li><li>Maintain accurate documentation of policies, audit reports, QIPs, and related research governance records.</li><li>Prepare analytical reports, dashboards, and presentations for management on research compliance, audit outcomes, and quality performance indicators.</li><li>Participate in research‑related committees and provide input on policy development, audit findings, and quality improvement initiatives.</li><li>Support awareness and training initiatives related to research policies, audit processes, and quality standards.</li><li>Contribute to continuous improvement initiatives aimed at enhancing research efficiency, compliance, and regulatory effectiveness.</li><li>Support and oversee clinical trial processes, including protocol review, ethical submissions, regulatory documentation, and study lifecycle tracking.</li><li>Ensure proper documentation, record keeping, and maintenance of research and clinical trial files in compliance with regulatory standards.</li><li>Support inspection and audit readiness for research and clinical trials, ensuring adherence to regulatory requirements.</li><li>Ensure confidentiality, integrity, and proper handling of all research‑related data and documentation.</li><li>Perform any other duties as assigned by the line manager.</li></ul><h3>Qualifications</h3><ul><li>Master’s degree in healthcare, research, public health, or related field.</li><li>Minimum 3–5 years of experience in research administration, policy development, audit, or quality improvement.</li><li>Experience in research governance, compliance, or regulatory environments.</li></ul><h3>Other Details</h3><p>Job Category: Administration</p><p>Advertiser: Dubai Health Authority</p><p>Required Nationality: All Nationalities (Priority for UAE National)</p><p>Monthly Salary: 20001‑30000</p><p>Schedule-Time: Full time</p></div>#J-18808-Ljbffr