Clinical Research Project Coordinator Job at CEDENT, Cincinnati, OH

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  • CEDENT
  • Cincinnati, OH

Job Description

Summary

We are looking for a Clinical Research Project Coordinator to support clinical trial management and drive the success of projects within a collaborative, fast-paced clinical research environment. Working closely with the Clinical Trial Management team, this role involves engaging in clinical trial activities, maintaining project timelines, and ensuring quality in regulatory and operational processes. Ideal candidates are detail-oriented professionals with strong organizational and time management skills, seeking to grow their careers in clinical research. Comprehensive training is provided, including virtual and hands-on learning experiences for individuals without prior clinical research experience.

Responsibilities
  • Engage in clinical trial management on a day-to-day basis.

  • Collaborate closely with the project Clinical Trial Manager (CTM) to deliver tasks with consistency and accuracy.

  • Compile and maintain project-specific status reports.

  • Interact with Sponsors, study sites, and internal associates.

  • Provide oversight and quality control of internal regulatory filing systems.

  • Manage study supplies to ensure seamless project execution.

  • Create and maintain project timelines to meet deliverables.

  • Coordinate project meetings and produce high-quality meeting minutes.

Requirements
  • Bachelor’s Degree in Life Sciences or a related field.

  • Excellent computer, organizational, and time management skills.

  • Research experience preferred, though not required.

Job Tags

Full time,

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