CRA I/II - Beijing/Shanghai/Guangzhou/Chengdu/Nanjing/Hangzhou/Tianjin/Changsha/Zhengzhou/Changchun
Remote · China
Job Summary
CRA I/II role supporting site qualification, initiation, monitoring, and close-out activities across multiple Chinese cities. Responsibilities include evaluating site performance, ensuring regulatory and ICH-GCP/GPP compliance, verifying informed consent, protecting subject data confidentiality, conducting source data review and data entry into CRFs, resolving queries, maintaining ISF/TMF alignment, and supporting investigator meetings and audit readiness. Requires delivering guidance to site staff, coordinating with sponsor teams, and managing travel up to 75%. Qualifications include a Bachelor’s degree or RN in a related field, knowledge of GCP/ICH and regulatory requirements, strong computer skills, and excellent communication and interpersonal abilities.
Required Qualifications
- Bachelor’s degree or RN in a related field or equivalent combination of education, training and experience
- Knowledge of Good Clinical Practice/ICH Guidelines and other applicable regulatory requirements
- Must demonstrate good computer skills and be able to embrace new technologies
- Excellent communication, presentation and interpersonal skills
- Ability to manage required travel of up to 75% on a regular basis
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