Associate Clinical Trial Manager

2 mesi fa


Lombardia, Italia Confidenziale A tempo pieno

Responsibilities Communicate and collaborate on global study activities; 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 reportswithin the clinical trial management system

Interact with the internal project team, Sponsor, study sites, and third-party vendors

Provide oversight and 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

Qualifications 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 Overview 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 global 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 4, people across almost 40 countries.



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