Medpace is currently seeking candidates with PhDs and/or Post-Doctoral Research experience for a full-time, office-based Associate Clinical Trial Manager (aCTM) to join our Clinical Trial Management team. The aCTM will be a part of the Clinical Trial Management team working with Project Coordinators and Clinical Trial Managers in performance of clinical trial management activities. Candidate must have a desire to transfer and apply analytical and academic skills in clinical project administration and management. Communicate and collaborate on global study activities; working closely with the project coordinator and clinical trial manager
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
Manage and perform quality control of our internal regulatory filing system
Provide oversight and management of study supplies
Create and maintain project timelines
Coordinate project meetings and produce quality minutes
PhD in Life Sciences




Fluency in English with solid presentation skills
Medpace is a full-service clinical contract research organization (CRO). We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Our mission is to accelerate the integral development of safe and effective medical therapeutics through its scientific and disciplined approach. We leverage local regulatory and therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, employing more than 5,000 people across 40+ countries.
Flexible work environment
Employee health and wellness initiatives
Continually recognized with CRO Leadership Awards from Life Science Leader magazine based on expertise, quality, capabilities, reliability, and compatibility

📌 Associate Clinical Trial Manager (Madrid)
🏢 Medpace
📍 Madrid