Research Coordinator – Chronic Kidney Disease

Mohammed Bin Rashid University of Medicine and Health Sciences (MBRU; www.mbru.ac.ae) is part of Dubai Health, the first integrated academic health system in the UAE. Dubai Health seeks to strengthen Dubai as a global leader in health care, medical education, research, and scientific innovation, to enhance the capabilities of Dubai’s healthcare sector. Dubai Health is managing and operating 54 sites, including 6 government hospitals, 26 ambulatory health centers, 20 medical fitness centers, Mohammed Bin Rashid University of Medicine and Health Sciences (MBRU), and Al Jalila Foundation.We are seeking a highly motivated and skilled Research Coordinator to join a multiprofessional team undertaking a study on the prevalence of chronic kidney disease (CKD) and the development of a CKD registry. This exciting role offers the opportunity to contribute to an innovative project with significant public health impact, working alongside clinicians, scientists, and public health professionals.The successful applicant will have a degree in Public Health or a related discipline (a Master’s degree is desirable), with strong skills in biostatistics, data management, coding and research coordination. The post-holder will play a central role in data collection, analysis, stakeholder engagement, and the preparation of reports and publications to support the development of the CKD registry.Job DescriptionJob Title: Research Coordinator – CKD Prevalence and Registry Development Location: Mohammed Bin Rashid University of Medicine and Health Sciences, Dubai, United Arab EmiratesReports to: Principal Investigator, CKD Registry Study Contract: 2 years full or part time (negotiable) Salary: To be agreedMain Duties and ResponsibilitiesLead data collection, entry, cleaning, and management of large health-related datasets.Conduct statistical analysis and support interpretation of data for reports and publications.Liaise with healthcare providers, research partners, and community stakeholders to support participant recruitment and registry engagement.Develop and maintain research documentation, protocols, and ethical governance submissions.Prepare interim and final project reports, presentations, and peer-reviewed manuscripts.Support the development of interactive data dashboards and visual reports to facilitate stakeholder engagement.Ensure data confidentiality, integrity, and compliance with data protection regulations.Provide training and supervision to junior staff or research assistants, where required.Essential CriteriaBachelor’s degree in Public Health, Data Science, Biostatistics, Epidemiology, or related discipline.Strong skills in statistical analysis and data interpretation.Ability to produce reports, presentations, and publications within set deadlines.Excellent problem-solving skills and attention to detail.Strong interpersonal skills with the ability to build and maintain collaborative relationships.Effective communication skills (oral and written).Strong planning, organising, and time management skills.Ability to delegate tasks and ensure timely delivery of outputs.Commitment to maintaining confidentiality of sensitive data.Desirable CriteriaMaster’s degree in Public Health, Epidemiology, Data Science, (Bio)statistics, or related field.Minimum 1 year of relevant research experience.Experience liaising with healthcare and community stakeholders.Experience in registry development.At least 6 months’ experience in healthcare data management.At least 6 months’ experience analysing large health-related datasets.Experience developing data dashboards and interactive reporting tools.Working knowledge of R, R Shiny, or equivalent statistical/programming software.Familiarity with Python, SQL, and Power BI.Understanding of data protection policies, confidentiality requirements, and IT/data security.How to ApplyPlease submit your CV and a cover letter outlining your suitability for the role via LinkedIn. Shortlisted candidates will be invited for interview.