Junior Study Start-Up Coordinator: Regulatory Submissions

Medpace; Cincinnati (OH); On-site; USD 45,000 - 65,000; Full time

Job summary

Medpace is seeking entry-level Study Start-Up Coordinators to join the Regulatory Submissions team in Cincinnati. You will manage timelines, collaborate with sites, and participate in a comprehensive training program to build a foundation in clinical research.

You will gain hands-on experience in trial start-up, TMF quality reviews, and IRB submissions while developing essential project coordination and communication skills in a dynamic, office-based setting.

Qualifications

• Bachelor's degree required; Life Sciences preferred.
• Some office experience is preferred.
• Excellent organizational and prioritization skills.
• Knowledge of Microsoft Office; strong attention to detail and communication skills.

Responsibilities

• Communicate with sites to collect essential documents before screening patients.
• Maintain and review trial documents in the Trial Master File (TMF).
• Prepare and assemble regulatory start-up submissions (IRBs, etc.).
• Maintain study start-up timelines through internal collaboration.

Skills

Organizational skills

Prioritization

Attention to detail

Oral and written communication

Education

Bachelor's degree in Life Sciences

Tools

Microsoft Office

Job description

Medpace is seeking entry-level Study Start-Up Coordinators to join the Regulatory Submissions team in Cincinnati. You will manage timelines, collaborate with sites, and participate in a comprehensive training program to build a foundation in clinical research.

You will gain hands-on experience in trial start-up, TMF quality reviews, and IRB submissions while developing essential project coordination and communication skills in a dynamic, office-based setting.