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الوصف الوظيفي Working with a delivery framework which includes the KSA Ministry of Health, the Cluster EDCSR will be accountable for the delivery of the following objectives: 1. Design and implement oversight mechanisms to monitor research study compliance, including all entities and components of the study (e.g., collaboration with sponsors, investigators and clinical trial teams, etc.); ensuring studies are conducted according to prescribed national/international standards, guidelines, regulations, and institutional polices. 2. Direct the provision of central administrative functions across all E1 health Cluster Clinical Research Service divisions including, but not limited to regulatory and protocol development, research committees, clinical trials coordination, and research training and education. 3. Execute strategic management of shared resources, facilities and knowledge/technology transfer across the E1 Health Cluster. 4. Prepare contingency research plans for emergencies and disasters, which address public health related issues. 5. Collaborate with E1 Public Health senior leadership to design, develop and implement epidemiology/public health research programs (i.e., acute and chronic disease) on a regional and national level. 6. Promote and facilitate interdisciplinary scientific research programs, and associated training. 7. Guide and direct investigators and research staff on relevant regulatory issues, using knowledge of international, national and other levels of policies and procedures and good clinical research practice. 8. Maintain strategically directed, scalable, efficient research administration teams, promoting a culture of high performance, quality and continuous improvement. 9. Ensures protocol compliance and patient safety of research activities at Health Networks involving protocol review and activation, screening, data management, study coordination and regulatory oversight. 10. Implement and maintain complex data management systems to code all research data; prepares comprehensive reports for key stakeholders. 11. Ensure timely, efficient, and accurate annual fiscal needs, and contracts are developed for all clinical trials, as needed, within the overall national guidelines and policies and make financial recommendations to the Chief of Research. 12. Design systems for the recruitment, training and supervision of scientist, researchers and research coordinators. 13. Hold to account Research partners to ensure high standards of excellence while providing support to meet these standards. 14. Performs a wide variety of functions as assigned in view of the evolving needs and opportunities within Eastern Cluster. 15. Performs other duties within the realm of his/her knowledge and ability as required. 16. Maintains confidentiality relating to all matters dealt. Uses great discretion at all times and ensure that no confidential material is released to unauthorized members of staff. 17. Follows all related policies and procedures. Participates in emergency and disaster procedures. Performs other duties within the realm of his/her knowledge and ability as required المهارات MD or PhD / Doctor or Masters of Education / MBA / Masters in social sciences / advanced degree in related field Experience 6+ years of relevant work experience inclusive of: · At least 3 years of which will have been spent in an Academic Medical Center or University Hospital. · Previous experience as a senior research scientist. · Developing and managing research initiatives for a healthcare organization · Experience in managing clinical research data collection, reporting, outcomes, quality improvement and standards/pathways. · Evidence of sustained relationships with industry, government and/or professional bodies and a proven track record of successfully navigating complex areas, especially advocacy, policy and the promotion of new thinking. Professional Licensure Actively registered and involved with an appropriate professional body/society تفاصيل الوظيفة https://www.bayt.com/ar/saudi-arabia/jobs/?page=4&jobId;=4201424 |
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