Responsibilities

• 1、Assist the project manager in daily clinical trial management, including document organization, data entry and verification.
• 2、Participate in subject screening, informed consent signing and follow-up work.
• 3、Maintain good communication with study sites, CROs and relevant departments to ensure smooth project progress.
• 4、Archive and manage clinical trial documents to ensure compliance with regulations and SOPs.

Requirements

• 1、Education: Bachelor’s degree or above; medical, pharmaceutical, nursing or related majors preferred.
• 2、Possess good communication skills and team spirit.
• 3、Candidates familiar with clinical trial processes and relevant regulations are preferred.
• 4、Work meticulously and responsibly, capable of adapting to a moderate work pace.