Clinical Trial Manager
Locations (fully office-based only): * Leuven, Belgium * Rotterdam, Netherlands * Munich, Germany * London (Hammersmith) or Stirling, UK Medpace is currently looking for Clinical Trial Managers (CTMs) to lead clinical research studies. Medpace is a scientifically led organization involved in full services for our clients, giving the Medpace project teams the empowerment to truly lead and execute clinical trials. Medpace works in a variety of therapeutic areas including oncology, cardiovascular, endocrine/metabolic, infectious disease, and CNS. Our physicians are truly integrated with the project teams. We have developed strong relationships with key PIs throughout the world in many indications. In addition, our structure allows the clinical trial management team to focus on operational execution of the project, versus spending excessive time on project financial tracking. The CTM position performs as project lead for multiservice clinical trials (some global in scope). The position interacts with sponsors and manages the timeline and all project deliverables. This role coordinates all services contracted for the study. CTMs are also responsible for leading a team of CRAs and managing project coordinators. Medpace is a global, full-service Clinical Research Organization (CRO) with a wide range of therapeutic expertise. Our headquarters are located in Cincinnati, Ohio, USA and we are active in over 35 countries across the globe. We are growing rapidly and are looking to add to our team. QUALIFICATIONS/REQUIREMENTS •Bachelor’s degree in a health related field (Master’s degree or PhD is preferred) ; •At least two years of clinical trial management experience WHAT TO EXPECT NEXT We look forward to receiving your application. A member of our recruitment team will review your qualifications. If interested, you will be contacted for an interview.