Clinical Trial Manager I - Shanghai
Hybrid · Shanghai, Shanghai, China
Job Summary
Clinical Trial Manager I role in Shanghai overseeing site qualification/initiation, interim monitoring, site management, and close-out activities (on-site or remotely). Responsible for ensuring regulatory, ICH-GCP, and GPP protocol compliance, performing source data review, CRF accuracy, IP handling, ISF/TMF management, audit readiness, and coordination with sponsor teams. Requires Bachelor’s degree or RN in a related field, strong communication skills, and ability to travel up to 75%. Works with cross-functional teams to support subject recruitment, data integrity, and regulatory adherence across global sites. This position uses a site-management mindset to drive quality and timelines in a dynamic biopharma environment.
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
Apply with one swipe on Sorce. We auto-fill applications and apply on your behalf — no cover letters, no 40-minute forms.
Hiring someone like this?
Get your role in front of qualified candidates on Sorce.