Medpace is a scientifically-driven, global, full-service clinical contract research organization (CRO) providing Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Medpace’s mission is to accelerate the global developmentof safe and effective medical therapeutics through its high-science and disciplined operating approach. We leverage local regulatory and deep therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, Medpace employs approximately 2,700 people across 36 countries.

Below are the positions we will be recruiting for at this event:


1. Clinical Research Associate (CRA)-located in Cincinnati, Ohio unless you have CRC experience.

Comprehensive training program that will provide you the resources and knowledge to monitor sites independently
Must be willing to travel 60-80%
Communicates with medical staff and clinical research physicians
Work with world class research sites


2. Project Coordinator (PC)-located in Cincinnati, Ohio

Partner with Clinical Trial Manager to coordinate dailystudy activities
Central point of contact for internal and external teammembers
Create and maintain project timeline


3. Regulatory Submissions Coordinator (RSC)-located in Cincinnati, Ohio

Assist with the start-up of clinical research sites
Collaborate with Institutional Review Boards (IRBs)
Prepare regulatory documents, including Informed Consent Forms


4. Clinical Trial Manager (CTM)-located in Cincinnati, Ohio

Postdoctoral Research or Healthcare research experience required
Managementof project timelines and all project deliverables
Responsible for leading internal prject team members

Please email Brooke Molloy at j.molloy@medpace.com for more information and to RSVP.