Office-Based Clinical Trial Project Coordinator

Medpace; Cincinnati (OH); On-site; USD 48,000 - 65,000; Full time

Benefits offered by this job

Health benefits

Retirement plan

PTO

On-site dining

Free on-site parking

Job summary

Medpace is seeking a full-time, office-based Project Coordinator to join our Clinical Trial Management team in Cincinnati, Ohio. You will work on a team to advance tasks, deliverables, and milestones that support our biotech clients across multiple therapeutic areas.

The role includes a 4–6 week training program combining virtual and hands-on learning. Ideal candidates hold a Bachelor’s Degree in Life Sciences, demonstrate strong organizational and time-management skills, and have a genuine

Qualifications

• Bachelor’s Degree in Life Sciences field 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 tasks with high 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.
• Coordinate project meetings and produce quality meeting minutes.

Skills

Time management

Computer proficiency

Research experience (preferred)

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, Ohio. You will work on a team to advance tasks, deliverables, and milestones that support our biotech clients across multiple therapeutic areas.

The role includes a 4–6 week training program combining virtual and hands-on learning. Ideal candidates hold a Bachelor’s Degree in Life Sciences, demonstrate strong organizational and time-management skills, and have a genuine