Job Description

Summary:

The role involves providing support for study coordination, data management, and regulatory activities within a Clinical Trials Office (CTO). This position ensures compliance with protocol guidelines, internal procedures, and regulatory requirements, while assisting multidisciplinary teams in research activities.

Responsibilities:

• Ensure all study requirements are documented and comply with internal and external regulations, following protocol guidelines.
  
• Maintain logs, including tracker submissions, and update the CTO OnCore database in a timely manner per CTO SOPs.
  
• Respond to queries promptly and accurately.
  
• Schedule and participate in monitoring visits.
  
• Attend multidisciplinary team program meetings as required.
  
• Assist multidisciplinary teams in various research activities.
  

Requirements

Requirements:

• Bachelor’s degree or an equivalent combination of education and experience.
  
• Medical and/or science education or experience is preferred.
  
• Proficiency in Microsoft Office Suite, including Excel and PowerPoint.
  
• Strong attention to detail and organizational skills.
  

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