Description
As a Clinical Research Coordinator, you will work with researchers to ensure compliance with regulations, SOPs, and study protocols.
Responsibilities:
- Assist researchers with feasibility surveys and questionnaire completion
- Support site initiation: assist with file submissions to ethics committees, drug dispensing, and site visits
- Help researchers with subject screening and study enrollment
- Collaborate with researchers to complete follow-up visits and procedures as required by the study protocol
- Manage investigational products, study materials, and laboratory samples at the study site
- Participate in investigator meetings, monitoring visits, audits, and other meetings as needed
- Assist researchers with study data archiving and submission to ethics committees or regulatory authorities
- Complete case report forms accurately and respond to queries
- Support site closure activities: close-out visits, investigational product return, and study material archiving
- Create and maintain daily work reports and other documents
- Travel to different sites or cities may be required
Requirements:
- Basic knowledge of clinical research and applicable regulations
- Familiarity with medical terminology
- Good communication and organizational skills
- Proficient in Microsoft Office software
- Fluent in Chinese, basic English proficiency
- Ability to work independently, prioritize tasks, and solve problems
- High level of confidentiality
Education and Experience:
- Associate's degree or higher in a related field (clinical medicine, pharmacology, nursing, etc.)
- Less than 1 year of experience as a clinical research coordinator
- Clinical research or pharmaceutical industry experience