CRA II

ICON · Shanghai, China

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Clinical OperationsFull-timeCompany career page

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What they're looking for

Bachelor's degree in scientific or healthcare-related field
Minimum 2 years of clinical research associate experience
In-depth knowledge of clinical trial processes, regulations, and ICH-GCP guidelines
Strong organizational and communication skills with attention to detail
Ability to work independently and collaboratively in fast-paced settings
Willingness to travel approximately 60% as required
Legal right to work in country where role is based

What you'll be doing

Conduct site qualification, initiation, monitoring, and close-out visits
Ensure protocol compliance, data integrity, and patient safety throughout trials
Collaborate with investigators and site staff to facilitate study conduct
Perform data review and resolve queries to maintain high-quality clinical data
Contribute to preparation and review of study documentation including protocols and reports

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RoleLantern checked active

RoleLantern checkedNeeds clarity

Date posted10 days ago

Last source check1 day ago

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