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上海, 中国其他地区, 临床及注册, 北京, 苏州 | 2021-10-04

Clinical Research Associate (CRA)

Job Title: Clinical Research Associate (CRA)
Location: Shanghai / Beijing / Guangzhou / Hangzhou / Nanjing / Suzhou / Chengdu /
Jinan / Changsha / Haerbin / Changchun / Shenyang / Zhengzhou / Xi’an

 

Primary

Act as principal link between the investigator and HMP for trial management, esp. on-site monitoring
 

Responsibilities

  • Be familiar with trial execution process of assigned trial
  • Be responsible for following activities:
    • Site selection
    • Prepare Site specific documents include but not limit to EC presentation slide, GCP office require documents, Inform Consent, study contract, site drug management manual, subject management matrix etc.
    • Site initiation
    • Site monitoring based on applicable monitoring plan
    • Site close out visit
    • Key personnel to coordinate with trial specific vendors to complete the trial related activities.
    • Complete all trial related reports within SOP defined timeline
  • Site level trial master file and investigator site file management
  • Deliver trial related training to site staffs
  • Update site status to project manager at timely manner
  • Prepare all required reports to line manager in a timely manner

 

Qualifications

  • At least 1 year clinical trial on site management experience
  • At least bachelor degree in Clinical Medicine or Pharmacy or related major
  • Good communication skill and team player
  • Good command of computer skill
  • Adequate verbal and written communication skills in English
  • Down-to-earth and hardworking spirit
  • Willingness to travel (up to 75%) of working time

 
If interested, please forward your resume to KellyL@hutch-med.com