PSI CRO is hiring a Site Management Associate (Clinical Trial)

Responsibilities

• Maintain databases and systems used for tracking study-related information.
• Act as the main point of contact for sites regarding vendor coordination, supply logistics, and access permissions.
• Handle extensive documentation tasks, including gathering, acquiring, organizing, and archiving materials.
• Liaise with internal departments and external partners to support study operations.
• Serve as the communication hub for clinical investigation sites involved in research initiatives.
• Coordinate resolution of site-specific questions, organize training, and facilitate access to third-party systems for site personnel.
• Oversee accurate processing and administration of financial transactions for sites and vendors.
• Manage incoming correspondence, including mail distribution and call routing.
• Support logistical arrangements for meetings and conferences.
• Draft meeting agendas and prepare summarized minutes for project discussions.