FSP Top Global Pharma
招聘要求：
1年左右临床试验助理相关经验背景，英语读写口语佳，CET-6优先
医药学临床等相关专业，有海外留学背景2024届毕业生可申请和考虑, 2025年毕业不考虑
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：北京市朝阳区中关村科技园电子城西区望京研发创新基地容达路21号楼
项目：
Global II/III期 肿瘤非肿瘤领域项目
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