Clinical Study Administrator – CTA
Parexel
full-time
Posted on:
Location Type: Remote
Location: Taiwan
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Tech Stack
About the role
- Coordinate and administer clinical studies from start-up to execution and closeout
- Manage trial and site administration tasks effectively
- Interface with investigators and external service providers
- Ensure compliance with regulatory documents and application processes
Requirements
- Clinical trial administration experience
- Knowledge of ICH-GCP guidelines
- Proficiency in document management systems
- Experience with stakeholder communication
- Ability to handle multiple tasks in a fast-paced environment
Benefits
- Health insurance
- 401(k) matching
Applicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills & Tools
clinical trial administrationdocument management systemsregulatory compliance
Soft Skills
stakeholder communicationmultitaskingtime management