Syneos FSP COS 临床试验助理

1年左右CTA经验背景，英语读写口语佳，CET-6优先

积极主动，踏实认真，注重细节，具有良好的团队合作经验

工作地点：上海静安寺CBD

项目：

Global II/III期 免疫呼吸心血管代谢中枢神经肿瘤领域

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

61 Responsible for performing activities in compliance with applicable Corporate and Clinical Operations Policies, Standard Operating Procedures and Work Instructions

61 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

61 Creates and assists with maintenance of Trial Master File (TMF) and project files, including participation in file audits

61 Prepares and maintains site manuals, reference tools and other documents

61 Maintains, updates, and inputs clinical tracking information into databases

61 Tracks incoming and outgoing clinical and regulatory documents and updates for investigator sites, studies, project team, or client

61 Manages shared mailbox, processes site requests and routes correspondence appropriately

61 Coordinates the ordering, packaging, shipping and tracking of site supplies and materials

61 Assists with coordination of team meetings, attends meetings and prepares accurate meeting minutes and action items

61 May handle receipt, tracking and disposition of Case Report Forms and Queries

61 Maintains overall awareness in the field of clinical research by completing all necessary and assigned training

QUALIFICATION REQUIREMENTS (please indicate if ‘preferred’)

61 Bachelor degree or above

61 Good communication and interpersonal skills

61 Ability to embrace new technologies

61 Minimal travel up to 25% may be required