Clinical Research Coordinator

• Oversee and manage clinical research studies from inception to conclusion
  
• Collect, document, and maintain study data in compliance with protocol requirements
  
• Conduct patient monitoring, including assessments of vital signs
  
• Supervise and train research personnel on study protocols and procedures
  
• Ensure compliance with FDA regulations and guidelines throughout the research process
  
• Review and maintain documentation about the research studies
  
• Collaborate with healthcare professionals to support patient care within the study's scope
  
• Assist in the collection, analysis, and interpretation of data for research projects
  

Requirements

• Bachelor’s degree in a relevant field (e.g., healthcare, life sciences) or International Medical Graduate
  
• Previous experience in clinical research or a related field
  
• Knowledge of medical terminology and clinical trial processes
  
• Familiarity with data management practices and electronic data capture systems
  
• Strong organizational skills with a high attention to detail
  
• Ability to work independently and collaboratively within a multidisciplinary team
  
• Excellent communication and interpersonal skills for effective collaboration
  
• Understanding of ethical considerations in clinical research