Research Assistant Clinical Research (UAE National)

• Help identify suitable study participants by reviewing eligibility against study-specific requirements.
  
  


• Guide participants through study information and support the informed consent process in line with approved procedures and assigned responsibilities.
  
  


• Coordinate participant appointments, follow-up visits, and communication with clinical teams.
  
  


• Collect and enter research information into electronic study databases, checking for missing details and inconsistencies.
  
  


• Maintain organized participant files, consent records, and essential study documentation.
  
  


• Support the preparation and tracking of ethics submissions, study updates, and approval records.
  
  


• Keep the research team informed about recruitment progress, participant follow-ups, and issues requiring attention.
  
  


• Help prepare study files for quality reviews, audits, and inspections.
  
  

Requirements

• A bachelor’s degree in Health Sciences, Nursing, Biology, Psychology, or a related discipline.
  
  


• At least one year of experience in clinical research or a relevant field.
  
  


• Practical exposure to patient interaction, participant screening, or study recruitment.
  
  


• Experience collecting research data, maintaining records, and working with electronic databases.
  
  


• An understanding of research ethics, participant confidentiality, and the importance of following study procedures.
  
  


• Strong attention to detail, clear communication, and the ability to manage multiple follow-ups.