12 set - Italia
Medpace
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.
A fantastic opportunity for recent PhD graduates to enter the industry, receive solid foundational training, work in an international environment, and develop their career in the research and development of cutting-edge therapeutics . Candidates should expect to have an intensive training period and show the desire and aptitude for an accelerated career path into Clinical Trial Management (CTM).
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
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
Ability to work in a fast-paced dynamic industry within an international team
Prior experience within the CRO or pharmaceutical industry not required but will be advantageous
Medpace is a full-service clinical contract research organization (CRO) providing phase l-lV clinical development services to the biotechnology, pharmaceutical, and medical device industries. Our mission is to accelerate the global development of safe and effective medical
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