Associate Clinical Trial Manager – PhD (Metabolic Research)
📍 Location: Cincinnati, Ohio
📂 Department: Clinical Trial Management
🆔 Job ID: 10750
Job Summary
Medpace, a global leader in Clinical Research Organization (CRO) services for biotechnology companies, is seeking PhD and/or Post-Doctoral Research professionals with expertise in Metabolic research for a full-time, office-based position as an Associate Clinical Trial Manager (aCTM) at our Cincinnati headquarters.
The aCTM will work as part of the Clinical Trial Management team, supporting Project Coordinators and Clinical Trial Managers in executing various project management activities. This position is ideal for candidates eager to apply analytical and academic skills in the clinical research and drug development industry.
This is an excellent opportunity for recent PhD graduates to gain foundational industry training, collaborate in an international environment, and accelerate their career in Clinical Trial Management (CTM).
Key Responsibilities
Communicate and collaborate on global study activities alongside Project Coordinators and Clinical Trial Managers.
Ensure timely and accurate completion of recurring project tasks.
Compile and maintain project-specific status reports within the Clinical Trial Management System (CTMS).
Liaise with internal teams, Sponsors, study sites, and third-party vendors.
Oversee and maintain quality control within internal regulatory filing systems.
Supervise and manage study supply logistics.
Develop and monitor project timelines and milestones.
Coordinate and document project meetings, producing high-quality meeting minutes.
Qualifications
PhD in Life Sciences (Metabolic research background preferred).
Excellent English communication and presentation skills.
Ability to work effectively in a fast-paced, international, and collaborative environment.
Prior experience in a CRO or pharmaceutical company is beneficial but not required.
Proficient in Microsoft Office (Word, Excel, Databases, Windows).
Strong organizational, analytical, and communication abilities.
About Medpace
Medpace is a full-service Clinical Research Organization (CRO) offering Phase I–IV clinical development services to the biotechnology, pharmaceutical, and medical device industries.
Our mission is to accelerate the development of safe and effective medical therapeutics through a disciplined and scientifically driven approach. We leverage global expertise across major therapeutic areas, including:
Oncology
Cardiology
Metabolic Diseases
Endocrinology
Central Nervous System (CNS) Disorders
Anti-viral and Anti-infective Research
🏢 Headquarters: Cincinnati, Ohio
🌍 Global Presence: 40+ countries
👥 Team Size: 5,000+ employees
Why Join Medpace?
People. Purpose. Passion.
Make a Difference Tomorrow — Join Us Today.
For over 30 years, Medpace has contributed to improving patient lives by advancing therapeutic innovations. The work you do today will directly impact the future of medicine and the well-being of people worldwide.
Cincinnati Campus Perks
Flexible, collaborative work environment
Competitive PTO starting at 20+ days
Comprehensive compensation and benefits package
Employee appreciation events and celebrations
Health and wellness initiatives including an on-site fitness center
Community engagement with local nonprofit organizations
Career growth and professional development through structured paths
Discounted tuition for University of Cincinnati online programs
Modern, eco-friendly campus with outdoor seating and workspace
Discounts on local sports, fitness, and attractions
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, reliability, and compatibility)
What to Expect Next
Once your application is submitted, a Medpace recruitment team member will review your qualifications.
If selected, you will be contacted with details about the next steps in the hiring process.
👉 Apply Now
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