Project Coordinator

Responsibilities

• Communicate with research sites to collect essential documents required for clinical trial participation
• Maintain and perform ongoing quality reviews of trial documents within the Trial Master File (TMF)
• Collect, review, organize, and assemble regulatory start-up submissions, including IRB submissions
• Maintain study start-up timelines through internal and external collaboration
• Provide guidance to team members to ensure compliance with applicable regulations and requirements
• Review pertinent regulations to develop proactive solutions to regulatory challenges

Requirements

• Bachelor's degree required (Life Sciences preferred)
• Experience within the healthcare or clinical research field preferred
• Excellent organizational and prioritization skills
• Proficiency with Microsoft Office
• Strong attention to detail
• Excellent oral and written communication skills

Benefits

• Competitive PTO packages starting at 20+ days
• Competitive compensation and benefits package
• Modern, eco-friendly campus with an on-site fitness center
• Structured career paths and professional growth opportunities
• Employee health and wellness initiatives
• Company-sponsored employee appreciation events

About the Company

Medpace is a full-service clinical contract research organization (CRO) providing Phase I-IV clinical development services to the biotechnology, pharmaceutical, and medical device industries. Headquartered in Cincinnati, Ohio, Medpace leverages local regulatory and therapeutic expertise to accelerate the global development of safe and effective medical therapeutics.