OverviewIn this full-time, office-based role you join the Clinical Trial Management team as an aCTM, applying your PhD or postdoctoral experience to support global clinical trials. You will collaborate with Project Coordinators and Clinical Trial Managers to deliver study activities with high accuracy. The position offers intensive training, international exposure, and a clear path toward leadership in CTM. This is an opportunity to translate rigorous research skills into practical trial management impact.

Retribuzione / Benefits

Flexible work environmentCompetitive compensation and benefits packageCompetitive PTO packagesStructured career paths with opportunities for professional growthCompany-sponsored employee appreciation eventsEmployee health and wellness initiatives

Responsabilità





Collaborate on global study activities with project team and sponsorsEnsure timely delivery of recurrent tasks with high accuracyCompile and maintain project-specific status reports in the CTM systemInteract with internal project team, Sponsor, study sites, and third-party vendorsManage and perform quality control of the internal regulatory filing systemProvide oversight and management of study suppliesCreate and maintain project timelinesCoordinate project meetings and produce quality minutes

Requisiti fondamentali

PhD in Life SciencesFluency in English with solid presentation skillsAbility to work in a fast-paced, international teamPrior CRO or pharmaceutical industry experience is advantageous but not requiredStrong communicationTeam collaborationExecutive presentation能力Clinical trial managementRegulatory filing systemsProject timeline creation

📌 Associate Clinical Trial Manager (PhD) - Neuroscience / Ophthalmology (Roma)
🏢 Medpace
📍 Roma