Clinical Research Project Coordinator Job at Medpace – Apply Now!
Medpace, a global leader in clinical research, is hiring a full-time Clinical Research Project Coordinator at its headquarters in Cincinnati, Ohio. This role is perfect for recent graduates with a degree in Life Sciences looking to enter the growing field of clinical trial management. With a structured 4–6 week training program, hands-on learning, and opportunities to work in therapeutic areas like Oncology, Infectious Diseases, and CNS, this role offers strong career growth in a collaborative, fast-paced environment.
About Medpace:
Medpace is a global, full-service CRO offering Phase I–IV clinical development services to the biotech, pharmaceutical, and medical device industries. Headquartered in Cincinnati, Medpace employs over 5,000 professionals across 40+ countries. The company focuses on scientific excellence and regulatory expertise, especially in oncology, cardiology, CNS, and infectious diseases. Medpace has earned recognition from Forbes and Life Science Leader for its leadership, quality, and employee satisfaction, making it a premier destination for clinical research professionals.
Job Details:
Position: Clinical Research Project Coordinator
Location: Cincinnati, Ohio
Department: Clinical Trial Management
Requisition ID: 10627
Job Summary
Medpace is seeking a full-time Project Coordinator to join our Clinical Trial Management team. This position involves working collaboratively on tasks and projects crucial to the company’s success. If you thrive in a fast-paced, clinical research environment and are looking to enhance your career, this opportunity is for you.
Responsibilities
- Engage in clinical trial management daily
- Work closely with project CTM for timely task delivery
- Compile project-specific status reports
- Interact with Sponsor, study sites, and internal associates
- Oversee and maintain internal regulatory filing system
- Manage study supplies
- Create and maintain project timelines
- Coordinate project meetings and produce quality meeting minutes
Qualifications
- Bachelor’s Degree in Life Sciences
- Strong computer, organizational, and time management skills
- Research experience preferred
Why Medpace?
- Flexible work environment
- Competitive PTO packages
- Company-sponsored events
- Employee health and wellness initiatives
- Community involvement
- Discounts on local attractions
- Career development opportunities
- Discounts on UC online programs
Keywords: Medpace, Cincinnati, Clinical Research, Project Coordinator, CRO, Clinical Trial Management, Biotech, Pharmaceutical, Medical Device Industries
