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項目： Global II/III期 免疫呼吸心血管代謝中樞神經(jīng)腫瘤領(lǐng)域

SUMMARY The position is responsible for providing clerical, administrative, and technical administrative support to one or more business units or clients within Clinical Operations. JOB RESPONSIBILITIES ? Responsible for performing activities in compliance with applicable Corporate and Clinical Operations Policies, Standard Operating Procedures and Work Instructions ? Assists Clinical Monitoring staff with site management activities, including serving as a Sponsor representative for sites on assigned studies, and communicating with sites to ensure compliance with protocol requirements, study procedures and relevant guidelines ? Creates and assists with maintenance of Trial Master File (TMF) and project files, including participation in file audits ? Prepares and maintains site manuals, reference tools and other documents ? Maintains, updates, and inputs clinical tracking information into databases ? Tracks incoming and outgoing clinical and regulatory documents and updates for investigator sites, studies, project team, or client ? Manages shared mailbox, processes site requests and routes correspondence appropriately ? Coordinates the ordering, packaging, shipping and tracking of site supplies and materials ? Assists with coordination of team meetings, attends meetings and prepares accurate meeting minutes and action items ? May handle receipt, tracking and disposition of Case Report Forms and Queries ? Maintains overall awareness in the field of clinical research by completing all necessary and assigned training QUALIFICATION REQUIREMENTS (please indicate if ‘preferred’) ? Bachelor degree or above ? Good communication and interpersonal skills ? Ability to embrace new technologies ? Minimal travel up to 25% may be required