Syneos FSP COS 临床试验助理

1 week ago

Guangzhou, Guangdong, China 赛纽仕医药咨询(上海)有限公司 Full time CN¥200,000 - CN¥400,000 per year

该职位来源于猎聘 FSP Top Global Pharma 招聘要求:

  • Life science related bachelor's degree or above
  • Good at communication, quick learner, with CTA or CRC related experience is preferred. For fresh graduates with high potential, it is also acceptable.
  • Candidates familiar with VBA or other automation technical skills (such as Power Apps, Power Automate, Python, etc.), proficient in using Excel, especially formula application will be given priority consideration. 应届硕士,有海外教育背景和IT编程技能优先,python, power automation, VBA etc.

积极主动,踏实认真,注重细节,具有良好的团队合作经验 英文流利 工作地点:徐汇漕河泾 项目: Global II/III期 肿瘤非肿瘤领域 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

  • 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

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