Clinical Trial Project Coordinator - Training & Growth

Medpace; Cincinnati (OH); On-site; USD 48,000 - 72,000; Full time

Job summary

Medpace is seeking a full-time, office-based Project Coordinator to join our Clinical Trial Management team in Cincinnati, OH. The role involves daily trial management activities and close collaboration with the CTM to ensure timely, accurate task delivery.

You will contribute to project timelines, status reports, and interactions with sponsors and sites. The company provides a 4–6 week training program with hands-on learning and onsite mentoring.

Qualifications

• Bachelor’s degree in Life Sciences required.
• Strong computer, organizational, and time management skills.
• Research experience preferred.

Responsibilities

• Engage in clinical trial management on a day to day level.
• Work closely with the project CTM for timely delivery of tasks consistently with a high degree of accuracy.
• Compile and maintain project-specific status reports.
• Interact with the Sponsor, study sites, and internal associates.
• Provide oversight and quality control of our internal regulatory filing system.
• Manage study supplies.
• Create and maintain project timelines; and
• Coordinate project meetings and produce quality meeting minutes.

Skills

Organization

Time management

Research experience

Computer skills

Education

Bachelor’s Degree in Life Sciences

Job description

Medpace is seeking a full-time, office-based Project Coordinator to join our Clinical Trial Management team in Cincinnati, OH. The role involves daily trial management activities and close collaboration with the CTM to ensure timely, accurate task delivery.

You will contribute to project timelines, status reports, and interactions with sponsors and sites. The company provides a 4–6 week training program with hands-on learning and onsite mentoring.