Associate Clinical Trial Manager Job for PhDs at Medpace – Apply Now!
Are you a PhD graduate or postdoc in life sciences looking to break into the clinical research industry? Medpace, a global leader in clinical trial management, is hiring Associate Clinical Trial Managers (aCTMs) in Cincinnati, Ohio. This role is ideal for PhDs specializing in Oncology, Hematology, or Radiopharmaceuticals who want to apply their analytical skills in managing global clinical trials. With a supportive training environment and structured career growth, Medpace is the perfect entry point into the CRO industry.
About Medpace
Medpace is a global, full-service Contract Research Organization (CRO) dedicated to accelerating clinical trials for pharmaceutical, biotechnology, and medical device industries. Headquartered in Cincinnati, Ohio, Medpace specializes in therapeutic areas like oncology, CNS, cardiovascular, infectious diseases, and more. With over 30 years of experience and operations in 40+ countries, Medpace delivers reliable, science-driven trial results through a collaborative and disciplined approach. The company emphasizes employee development, diversity, and scientific excellence, making it a top choice for launching and growing a career in clinical research.
Job Details:
Job Role: Associate Clinical Trial Manager – PhD – Postdoctoral – Oncology, Hematology, Radiopharm
Location: Cincinnati, Ohio
Categories: Clinical Trial Management
Job Req Id: 10748
Job Summary
Medpace, a leading CRO for biotech companies, is hiring PhDs or postdocs in Oncology, Hematology, or Radiopharm for a full-time, office-based Associate Clinical Trial Manager (aCTM) role. The position supports clinical project management activities and offers PhD graduates a strong entry point into the industry with hands-on training, international exposure, and a fast-tracked career path in Clinical Trial Management.
Responsibilities
- Communicate and collaborate on global study activities, working closely with the project coordinator and clinical trial manager.
- Ensure timely delivery of recurrent tasks consistently with a high degree of accuracy;
- Compile and maintain project-specific status reports within the clinical trial management system.
- Interact with the internal project team, Sponsor, study sites, and third-party vendors;
- Provide oversight and quality control of our internal regulatory filing system;
- Provide oversight and management of study supplies;
- Create and maintain project timelines; and
- Coordinate project meetings and produce quality minutes.
Qualifications
- PhD in Life Sciences;
- Fluency in English with solid presentation skills;
- Ability to work in a fast-paced, dynamic industry within an international team;
- Prior experience within the CRO or pharmaceutical industry is not required, but will be advantageous.
- Excellent computer (word-processing, databases, Excel, Windows), organizational, and communication skills.
Keywords: Clinical research job for PhDs, Entry-level PhD job in clinical trials, PhD clinical trial associate, Life science PhD job in CRO, Clinical project manager PhD, Postdoc to industry transition, Clinical trial career for researchers
