Director, Clinical Trial Management
Location: Cincinnati, Ohio (Remote options available for qualified candidates)
Category: Clinical Trial Management
Job ID: 10699
Position Overview
Medpace, a leading full-service Clinical Research Organization (CRO), is seeking a Director of Clinical Trial Management to join our growing team. This senior-level role offers the opportunity to lead high-impact projects in key therapeutic areas, including Oncology/Hematology, Cardiovascular/Metabolic, Infectious Disease, and Neuroscience.
This position can be based in Cincinnati, OH, Dallas, TX, Denver, CO, or remotely with relevant experience. We offer a highly competitive salary, performance-based bonuses, and equity grants for senior associates.
Key Responsibilities
Provide overall leadership and accountability for day-to-day clinical trial operations, ensuring adherence to ICH/GCP guidelines and applicable regulatory standards.
Serve as the primary Sponsor contact for operational project-specific issues and deliverables.
Maintain comprehensive knowledge of protocol, therapeutic area, and study indication.
Lead and oversee cross-functional project teams, ensuring proper training, task allocation, and timely deliverables.
Review and provide input on study protocols, edit check specifications, data analysis plans, and final study reports as applicable.
Develop and implement operational project plans, including risk assessment and mitigation strategies.
Manage study vendors and external collaborators to ensure high-quality deliverables.
Monitor site quality, monitoring activities, and project timelines, proactively addressing issues as they arise.
Participate in bid defense and client presentations.
Qualifications and Experience Required
Bachelor’s degree in a health-related field; advanced degree preferred (PharmD, MPH, or equivalent).
5+ years of experience as a Project Manager or Clinical Trial Manager within a CRO.
Proven experience managing Phases 1-4 clinical trials, with Phases 2-3 preferred.
Strong leadership and team management skills, with experience overseeing cross-functional teams.
Demonstrated ability to manage complex project timelines, vendors, and risk mitigation strategies.
Excellent communication, problem-solving, and decision-making skills.
Bid defense experience is highly desirable.
Why Join Medpace?
Medpace is committed to accelerating the global development of safe and effective therapeutics across all major therapeutic areas. As part of our team, you will:
Contribute to meaningful clinical research impacting patients worldwide.
Access structured career paths and professional growth opportunities.
Participate in a flexible work environment with competitive compensation and benefits.
Engage in company-sponsored health, wellness, and employee appreciation programs.
Collaborate in a modern, eco-friendly work environment with on-site amenities in Cincinnati, including fitness facilities.
Employee Perks – Cincinnati Campus
Flexible work schedules with partial remote options.
PTO packages starting at 20+ days annually.
Competitive salary and benefits, including equity grants and bonus programs.
Community engagement with local nonprofits and wellness initiatives.
Discounts on local sports, fitness gyms, and entertainment.
Tuition discounts for University of Cincinnati online programs.
Awards & Recognition
Top Workplace 2024 – The Cincinnati Enquirer
Forbes America’s Most Successful Midsize Companies (2021–2024)
CRO Leadership Awards from Life Science Leader magazine for quality, capability, and reliability
Next Steps
Qualified candidates will be reviewed by our recruitment team. Shortlisted applicants will be contacted with details on the next steps of the selection process.
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