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