中文

Position Title:Clinical Research Associate and Intern
Department:Clinical Operations
Location:Wuhan, Chengdu, etc.

Position Summary

Responsible for the site monitoring and coordination of all aspects of clinical studies assigned in accordance with ICH-GCP, and local regulatory requirements, and SOPs of Sponsor and /or dMed. Be flexible to manage various projects and capable to handle different therapeutic areas and different studies.

Key Responsibilities

Study documents management

  • Initial preparation such as printing EC submission binder
  • Support on investigator documents preparation and distribution
  • Paper documents filing;
  • e-documents filing on related system
  • Study supply management

  • Coordinate with clinical trial support team on supply purchasing when study initiation
  • Supply delivery and tracking
  • Study system management

  • Documents submission and update
  • Run system report and support on analysis
  • Site management

  • Draft contract with template
  • Signing off tracking
  • Coordinate with CRAs on site documents and date collection
  • Initial meeting preparation and on site support
  • Others

  • Record meeting minutes
  • Support CRAs on finance reimbursement

  • Education and Key Competency Requirement
    Professional Experience & Education Requirement

  • Bachelor degree or above
  • Priority will be given to medical or pharmaceutical education background others also can be considered
  • Good teamwork
  • Good communication skill; service consciousness; response capability
  • Familiar with office software WORD/PPT/EXCEL etc.
  • Fluency in oral and writing English
  • CET 4 or above

  • Time requirements

  • Working 3-4 days per week
  • 6 months internship
  • Apply for the position
    Submit

    China:
    298 Xiangke Road, 3/F, 301-305, Zhangjiang Hi-Tech Park, Pudong, Shanghai 201210, China
    Tel: +86 21 5090 0085 Fax: +86 21 6875 5515
    US:
    261 Madison Avenue, 24th fl. New York, NY 10016 US
    Phone: +1-212-681-2100
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