Clinical Research Associate II
Parexel
full-time
Posted on:
Location Type: Remote
Location: Remote • 🇨🇳 China
Visit company websiteJob Level
JuniorMid-Level
Tech Stack
Google Cloud Platform
About the role
- Monitoring and Management of Investigator Sites
- Conducts source data verification (SDV)
- Identifies and manages issues impacting study conduct
- Ensures compliance with ICH/GCP and local laws
- Responsible for site management from selection to closeout
Requirements
- At least 1.5 years (2 years preferable) of Clinical Monitoring/ Site Management experience
- Good knowledge of ICH/GCP, relevant international and local regulations relating to Clinical Research
- Proficient in Chinese, good command of written and spoken English is required
- Degree in Life Science, Nursing, Pharmacy, or other relevant education background
Benefits
- Health insurance
- Retirement plans
- Paid time off
- Flexible work arrangements
- Professional development
Applicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard skills
Clinical MonitoringSite ManagementSource Data Verification
Soft skills
Problem SolvingCommunication