Associate Clinical Trial Manager – PhD / Postdoctoral (Oncology, Hematology, Radiopharm)
Location: Irving (Dallas), Texas
Department: Clinical Trial Management
Job ID: 10749
Job Summary
Medpace, a global leader in clinical research for biotechnology companies, is seeking PhD and/or Postdoctoral candidates with research experience in Oncology, Hematology, or Radiopharmaceuticals for the position of Associate Clinical Trial Manager (aCTM).
This full-time, office-based role offers recent PhD graduates an excellent opportunity to transition into the clinical research industry, receive comprehensive training, and develop strong foundational skills in clinical project administration and management.
The aCTM will work closely with Project Coordinators and Clinical Trial Managers (CTMs) to support global clinical studies and gain hands-on experience in project management activities.
Key Responsibilities
Communicate and collaborate on global study activities with project coordinators and CTMs.
Ensure timely and accurate delivery of assigned project tasks.
Compile and maintain project-specific status reports in the Clinical Trial Management System (CTMS).
Coordinate with internal teams, sponsors, investigative sites, and third-party vendors.
Oversee and perform quality control of internal regulatory filing systems.
Manage and track clinical study supplies.
Create and maintain project timelines to ensure smooth trial progression.
Organize project meetings and prepare comprehensive meeting minutes.
Qualifications
Education: PhD in Life Sciences (e.g., Oncology, Hematology, Radiopharm, or related field).
Experience:
Previous experience in a CRO or pharmaceutical company is not required but considered an asset.
Skills:
Excellent English fluency and presentation skills.
Strong organizational, communication, and analytical abilities.
Proficient in Microsoft Office (Word, Excel, PowerPoint, databases, Windows).
Ability to work efficiently in a fast-paced, international team environment.
About 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 a scientific and disciplined approach.
Headquarters: Cincinnati, Ohio
Employees: 5,000+ across 40+ countries
Therapeutic Expertise: Oncology, Cardiology, Endocrinology, CNS, Metabolic Disease, Anti-Viral, and Anti-Infective
Why Join Medpace?
People. Purpose. Passion. Make a Difference Tomorrow. Join Us Today.
For over three decades, Medpace has advanced breakthrough therapies that improve lives across numerous disease areas. Join a team where science, integrity, and innovation shape the future of healthcare.
Dallas Campus Perks
Flexible work environment
Competitive PTO packages (starting at 20+ days)
Competitive salary and benefits package
Company-sponsored employee appreciation events
Health and wellness initiatives
Community involvement with nonprofit organizations
Discounts on local sports games, gyms, and attractions
Modern, eco-friendly campus with on-site fitness center
Free on-site parking and outdoor workspaces
Clear, structured career growth paths
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 qualifications.
If you’re a good fit, you’ll be contacted with details regarding the next steps in the hiring process.
Apply Now
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