Associate Director, Clinical Trial Management
Location: Cincinnati, Ohio (Remote options available for qualified candidates)
Category: Clinical Trial Management
Job ID: 10573
Position Overview
Medpace, a leading global Clinical Research Organization (CRO) serving biotechnology and pharmaceutical companies, is seeking an Associate Director of Clinical Trial Management. This senior-level role offers the opportunity to oversee clinical trials across multiple therapeutic areas and ensure operational excellence.
We provide remote flexibility for candidates with relevant experience and offer a highly competitive salary, performance-based bonuses, and equity grants for senior associates.
Key Responsibilities
Lead and ensure accountability for day-to-day clinical trial operations in compliance with contract obligations, ICH/GCP guidelines, and applicable regulatory requirements.
Serve as the primary Sponsor contact for operational project-specific issues and study deliverables.
Maintain in-depth expertise of study protocols, therapeutic areas, and indications across Oncology/Hematology, Cardiovascular, Renal, Gastrointestinal, Endocrine/Metabolic, Infectious Disease, Neuroscience, and more.
Provide cross-functional oversight of internal project teams, including training, task allocation, and performance monitoring.
Review and provide input on study protocols, edit check specifications, data analysis plans, and final study reports.
Develop and execute operational project plans, including risk assessment and mitigation strategies.
Manage study vendors and ensure compliance with quality standards.
Oversee site quality and monitoring deliverables throughout the project lifecycle.
Qualifications and Experience Required
Bachelor’s degree in Health Sciences, Life Sciences, or related field; Advanced degree preferred.
5+ years of experience as a Clinical Trial or Project Manager within a CRO.
Proven experience managing Phase 1-4 clinical trials (Phase 2-3 preferred).
Experience managing project timelines and cross-functional teams.
Bid defense experience preferred.
Strong leadership, communication, and decision-making skills.
Why Join Medpace?
Medpace accelerates the global development of safe and effective medical therapeutics across oncology, cardiology, metabolic disease, CNS, anti-infective, and other therapeutic areas. As an Associate Director, you will:
Lead teams that directly impact patient outcomes worldwide.
Influence strategic decisions and clinical trial execution at a global level.
Access structured career growth paths and leadership development programs.
Work in a flexible, supportive environment with competitive compensation and benefits.
Cincinnati Campus Benefits
Flexible work schedules and remote options for qualified candidates.
PTO packages starting at 20+ days annually.
Company-sponsored employee appreciation and wellness programs.
Discounts on local sports events, fitness centers, and attractions.
Modern, eco-friendly campus with on-site fitness facilities.
Community engagement initiatives with local nonprofit organizations.
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 – Life Science Leader magazine, recognized for expertise, quality, capabilities, and reliability
Next Steps
Qualified applicants will be reviewed by our recruitment team. Shortlisted candidates will be contacted with details for the next stage of the selection process.
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