Associate Clinical Trial Manager – PhD / Postdoctoral (Oncology, Hematology, Radiopharm)
Location: Cincinnati, Ohio
Department: Clinical Trial Management
Job ID: 10748
Job Summary
Medpace, a leading global Clinical Research Organization (CRO) for biotech companies, is seeking highly motivated individuals with PhD and/or Postdoctoral research experience in Oncology, Hematology, or Radiopharm for the position of Associate Clinical Trial Manager (aCTM).
This is a full-time, office-based position that offers a unique opportunity for recent PhD graduates to transition from academia into the clinical research industry. The aCTM will support Project Coordinators and Clinical Trial Managers (CTMs) in executing and overseeing global clinical trials, contributing to the development of innovative therapies.
Medpace provides a comprehensive training program, preparing candidates for an accelerated career path in Clinical Trial Management.
Key Responsibilities
Communicate and collaborate on global study activities, working closely with project coordinators and CTMs.
Ensure timely and accurate completion of recurring project tasks.
Compile and maintain project-specific status reports within the Clinical Trial Management System (CTMS).
Coordinate with internal project teams, Sponsors, study sites, and third-party vendors.
Oversee and ensure quality control of internal regulatory filing systems.
Manage and track study supplies to ensure adequate inventory.
Create, maintain, and monitor project timelines.
Organize project meetings and prepare detailed meeting minutes.
Qualifications
Education: PhD in Life Sciences (e.g., Oncology, Hematology, Radiopharm, or related field).
Experience:
Prior CRO or pharmaceutical industry experience is not required but considered advantageous.
Skills:
Excellent English fluency and presentation skills.
Strong organizational, analytical, and communication abilities.
Proficiency in Microsoft Office (Word, Excel, PowerPoint, databases, Windows).
Ability to thrive in a fast-paced, international environment.
About Medpace
Medpace is a full-service Clinical Contract Research Organization (CRO) providing Phase I–IV clinical development services to biotechnology, pharmaceutical, and medical device industries.
Our mission is to accelerate the global development of safe and effective medical therapeutics through a scientific and disciplined approach.
Headquarters: Cincinnati, Ohio
Employees: 5,000+ across 40+ countries
Therapeutic Expertise: Oncology, Cardiology, Metabolic Diseases, Endocrinology, CNS, Anti-viral, Anti-infective
Why Join Medpace?
People. Purpose. Passion. Make a Difference Tomorrow. Join Us Today.
For over 30 years, Medpace has contributed to breakthroughs that positively impact patients and families worldwide. Be part of a team that combines science, purpose, and innovation to transform the future of healthcare.
Cincinnati Campus Perks
Flexible work environment
Competitive compensation and benefits package
Generous PTO (starting at 20+ days)
Company-sponsored employee appreciation events
Comprehensive health and wellness initiatives
Community involvement with local nonprofits
Discounts on sports games, gyms, and attractions
Modern, eco-friendly campus with on-site fitness center
Structured career paths with clear growth opportunities
Discounted tuition 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 (Expertise, Quality, Capabilities, Reliability, Compatibility)
Next Steps
A Medpace recruitment team member will review your application.
If your qualifications match the role, you will be contacted with details about the next steps in the hiring process.
Apply Now
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