Junior Clinical Research Project Coordinator – Training Provided

Medpace; Cincinnati (OH); On-site; USD 52,000 - 75,000; Full time

Benefits offered by this job

On-site mentors

Career development and onboarding

Health, wellness, retirement, and PTO

Office-based with eligible WFH after培训

Job summary

Medpace is a leading CRO seeking a full-time, office-based Project Coordinator to join our Clinical Trial Management team in Cincinnati, OH. The position includes a 4–6 week training program combining virtual and hands-on learning, especially for those without prior clinical research experience.

You will engage daily in trial management, coordinate with the CTM, prepare status reports, interact with sponsors and sites, oversee regulatory filing, manage study supplies, and maintain timelines.

Qualifications

• Bachelor’s Degree in Life Sciences field is required.
• Excellent 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 recurrent 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

Time management

Organizational skills

Computer skills

Research experience

Education

Bachelor’s Degree in Life Sciences

Job description

Medpace is a leading CRO seeking a full-time, office-based Project Coordinator to join our Clinical Trial Management team in Cincinnati, OH. The position includes a 4–6 week training program combining virtual and hands-on learning, especially for those without prior clinical research experience.

You will engage daily in trial management, coordinate with the CTM, prepare status reports, interact with sponsors and sites, oversee regulatory filing, manage study supplies, and maintain timelines.