Clinical Trials Associate Project Manager
Pubblicato il 23-09-2026 - Medpace in Pavia
Overview As an Associate Clinical Trial Manager at Medpace, you join the Clinical Trial Management team to help oversee global trial activities and ensure timely, accurate execution. You will collaborate with project coordinators, clinical trial managers, sponsors, and sites, applying your analytical and academic background to clinical project administration. This role offers intensive training, international exposure, and a clear path toward advanced CTM responsibilities.
You'll work on coordinating study timelines, quality control, and stakeholder communications to advance cutting-edge therapeutics. This is a hands-on entry into industry with meaningful impact on patient outcomes.
Retribuzione / Benefits Flexible work environment Competitive compensation and benefits package Competitive PTO packages Structured career paths with opportunities for professional growth Company-sponsored employee appreciation events Employee health and wellness initiatives Responsabilità Communicate and collaborate on global study activities with project coordinator and clinical trial manager Ensure timely delivery of recurring tasks with high accuracy Compile and maintain project-specific status reports in the CTM system Interact with internal project team, Sponsor, study sites, and third-party vendors Manage and perform quality control of the internal regulatory filing system Provide oversight and management of study supplies Create and maintain project timelines Coordinate project meetings and produce quality minutes Requisiti fondamentali PhD in Life Sciences Fluency in English with strong presentation skills Ability to work in a fast-paced, international team Prior CRO or pharmaceutical industry experience is advantageous but not required strong communication team collaboration ability to work under pressure clinical trial management regulatory filing processes project timeline management