Clinical Trial Project Manager

4 weeks ago

Cincinnati, Ohio, United States Medpace Full time
Clinical Trial Project Manager Job Summary

Medpace is seeking a Clinical Trial Project Manager to lead full-service global clinical trials for Medical Devices. The ideal candidate will have experience in Medical Devices for Metabolic, Cardiovascular, Diabetes, and more. This role involves interacting with sponsors and managing project timelines and deliverables.

Responsibilities:
  • Lead a clinical team to provide daily work direction to clinical study team members to support clinical site needs and meet sponsor goals and timelines.
  • Coordinate and manage project start-up, maintenance, and close-out activities.
  • Maintain ongoing sponsor contact for project-specific issues by serving as the primary contact for sponsors and project team members.
  • Track study status and progress according to milestones, identify potential issues or challenges, and work with the team to develop solutions.
  • Provide project management oversight of Project Coordinators, Clinical Trial Assistants, Clinical Research Associates, and other clinical study team members.
  • Develop study management tools, including communication plans, clinical monitoring plans, patient recruitment and retention plans, and other study-specific documents and management tools.
  • Communicate changes in scope to sponsor clinical teams and Medpace account managers.
  • May be responsible for other projects and responsibilities as assigned.
  • Provide input on the following (as applicable): study protocol/clinical investigation plan, edit check specifications, data analysis plan, data clean-up results, analysis, and final study report.
Qualifications:
  • Bachelor's degree in Life Sciences or a related field and a minimum of 3 years of related medical device industry experience, or Master's degree in Life Sciences or a related field and a minimum of 2 years of related medical device industry experience.
  • Prior experience with medical device trials is preferred.
  • CRO experience is preferred.
  • Exceptional communication skills (oral and written).
  • High attention to detail and quality standards.
  • Strong time and project management skills.
  • Demonstrate measurable knowledge of Good Clinical Practice for medical device trials in the US (21 CFR 812 and other sections) and/or Europe (ISO 14155), and local regulations.
  • Proficient with all Microsoft Office applications (Word, Excel, PowerPoint, Project, etc.).
Why Medpace?

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. Our mission is to accelerate the global development of safe and effective medical therapeutics through our 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, we employ over 5,000 people across 40+ countries.

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.

Cincinnati Perks

  • Cincinnati Campus Overview
  • Hybrid work-from-home options (dependent upon position and level)
  • Competitive PTO packages, starting at 20+ days
  • Competitive compensation and benefits package
  • Flexible work schedule
  • Company-sponsored employee appreciation events
  • Employee health and wellness initiatives
  • Community involvement with local nonprofit organizations
  • Discounts on local sports games, fitness gyms, and attractions
  • Modern, eco-friendly campus with an on-site fitness center
  • Structured career paths with opportunities for professional growth
  • Discounted tuition for UC online programs

Awards

  • Named a Top Workplace in 2024 by The Cincinnati Enquirer
  • 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.

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