Clinical Research Associate ensuring high‑quality clinical trial execution across all study phases. Supporting patient safety and protocol compliance while collaborating with investigative sites.
About the role
- Clinical Research Associate in PAREXEL managing protocol compliance across clinical sites in China. Building relationships with site staff and conducting evaluations to ensure study success.
Responsibilities
- Act as PAREXEL’s direct contact with assigned sites
- Build relationships with investigators and site staff
- Evaluate site recruitment plan in collaboration with the site staff
- Ensure compliance with ICH-GCP and applicable international and local regulations
Requirements
- Site Management experience or equivalent experience in clinical research
- Understanding of clinical trials methodology and terminology
- Educated to degree level (biological science, pharmacy, or other health-related discipline preferred) or equivalent nursing qualification or other equivalent experience
Benefits
- Health insurance
- 401(k) plan
- Paid time off
- Professional development opportunities
Job title
Job type
Experience level
Salary
Not specified
Degree requirement
Tech skills
Location requirements
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