Site Specialist I
ICON · Beijing, China
Clinical OperationsFull-timeCompany career page
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Role summary
Clinical research organization seeks a Site Specialist I to conduct site qualification, monitoring, and close-out activities for clinical trials in Beijing. The role involves ensuring protocol compliance, data integrity, patient safety, and collaborating with investigators to support study conduct.
What they're looking for
- Bachelor's degree in scientific or healthcare-related field
- Minimum 2 years of experience as a site specialist or SSU
- In-depth knowledge of clinical trial processes and ICH-GCP guidelines
- Strong organizational and communication skills with attention to detail
- Ability to work independently and collaboratively in fast-paced environment
- Legal right to work in China
What you'll be doing
- Conduct site qualification, initiation, monitoring, and close-out visits for trials
- Ensure protocol compliance, data integrity, and patient safety throughout study process
- Collaborate with investigators and site staff to facilitate study conduct
- Perform data review and resolution of queries to maintain clinical data quality
- Prepare and review study documentation including protocols and clinical study reports
Privacy & handoff
This role links to ICON's own application system. RoleLantern records your interest and checks the link, but the application happens on the employer's site and status updates may not come back to us. Clicking apply does not mark you as applied automatically.