Medpace

Job Summary

Our imaging services are growing rapidly, and we are currently seeking a full-time, office-based Project Coordinator to join our team. If you want an exciting career where you use your previous expertise and can develop and grow your career even further, then this is the opportunity for you.

Responsibilities

• Review incoming medical imaging data for clinical trials for initial quality standards.
• Draft and maintain study-related documents (in English)
• Contact with sites (hospitals), all around the word for qualification, follow up and queries
• Quality control of the received imaging data and transmittal forms
• Work on several projects with different teams (Cincinnati and France)
• Support of the Project Manager tasks such as for data export request and QC
• Overall meeting support: organization, agenda, meeting minutes, attendance sheet
• Coordinate shipments
• Interact with Project Managers, Project Assistant and Imaging Technologists
• Report to the Project Manager

Qualifications

• Bachelor's degree in science or medical related field, clinical trials or related field
• Prior experience with clinical trials is a plus (clinical research associate are welcome to apply)
• Prior experience as a Project Coordinator within a CRO or a pharma company is preferred
• Knowledge of Medical Imaging desirable but not mandatory
• Understanding of International Conference on Harmonization (ICH)-Good Clinical Practice (GCP) guidelines and other regulatory requirements that may impact clinical trials (FDA, EMA, etc.)
• Excellent computer (word-processing, databases, Excel, Windows), organizational, and communication skills
• Good level of English. Should be able to communicate fluently and write documents.

No travel.

We kindly request to submit CV in English.

Medpace Overview

Medpace is a full-service clinical contract research organization (CRO). We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through its scientific and disciplined approach. We leverage local regulatory and therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, employing more than 5,000 people across 40+ countries.

Why Medpace?

People. Purpose. Passion. Make a Difference Tomorrow. Join Us Today.

The work we’ve done over the past 30+ years has positively impacted the lives of countless patients and families who face hundreds of diseases across all key therapeutic areas. The work we do today will improve the lives of people living with illness and disease in the future.

Medpace Perks

• Flexible work environment 
• Competitive compensation and benefits package
• Competitive PTO packages
• Structured career paths with opportunities for professional growth
• Company-sponsored employee appreciation events
• Employee health and wellness initiatives

Awards

• Recognized by Forbes as one of America's Most Successful Midsize Companies in 2021, 2022, 2023 and 2024
• Continually recognized with CRO Leadership Awards from Life Science Leader magazine based on expertise, quality, capabilities, reliability, and compatibility

What to Expect Next

A Medpace team member will review your qualifications and, if interested, you will be contacted with details for next steps.

EO/AA Employer M/F/Disability/Vets