Strategic Study Start-Up Coordinator (CRC Expert)

Medpace; Cincinnati (OH); On-site; USD 55,000 - 75,000; Full time

Benefits offered by this job

Competitive compensation

Health benefits

Retirement plan

PTO

WFH flexibility

Social events

Job summary

Medpace is seeking a Clinical Research Coordinator for Cincinnati, OH, to support study start-up activities and trial management. This role involves coordinating with research sites and internal teams to ensure timely, compliant initiation of clinical studies.

You will maintain TMF quality, assist with regulatory submissions, and help guide teams through regulatory requirements. A Life Sciences degree and 1–2 years of study coordination experience are ideal.

Qualifications

• Bachelor's degree in Life Sciences required.
• 1–2 years of prior experience as a study coordinator or in the pharmaceutical industry, study start-up experience preferred.
• Excellent organization and communication skills; ability to manage multiple tasks.
• Knowledge of Microsoft Office (Word, Excel, PowerPoint) and related tools.

Responsibilities

• Communicate with research sites to collect essential regulatory documents before site screening.
• Maintain and review trial documents in the Trial Master File (TMF).
• Prepare and submit regulatory start-up documents, including IRB submissions.
• Maintain timelines for study start-up across internal and external teams.
• Provide guidance to internal/external members to ensure regulatory compliance.
• Review regulations to develop proactive solutions for regulatory challenges.

Skills

Communication

Organization

MS Office

Team coordination

Education

Bachelor's degree in Life Sciences

Tools

Microsoft Office

Job description

Medpace is seeking a Clinical Research Coordinator for Cincinnati, OH, to support study start-up activities and trial management. This role involves coordinating with research sites and internal teams to ensure timely, compliant initiation of clinical studies.

You will maintain TMF quality, assist with regulatory submissions, and help guide teams through regulatory requirements. A Life Sciences degree and 1–2 years of study coordination experience are ideal.