| 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