Clinical Research Coordinator I Job at Cedent Consulting Inc, Detroit, MI

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  • Cedent Consulting Inc
  • Detroit, MI

Job Description

Job Description

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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