Clinical Research Associate – FSP
Parexel
full-time
Posted on:
Location Type: Remote
Location: Brazil
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About the role
- Responsible for site management and monitoring of clinical trials
- Ensure patient safety and quality study execution
- Manage operational aspects from site activation to database lock
- Serve as the primary contact for investigator sites
- Monitor site level adverse events and resolve protocol-related issues
Requirements
- 1+ years of monitoring experience
- Knowledge of clinical trial methodologies
- Demonstrated knowledge of global and local regulatory requirements
- Bachelor's degree in life sciences or equivalent
- Must be fluent in English and in the native language(s) of the country
Benefits
- Health insurance
- Retirement plans
- 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 & Tools
monitoring experienceclinical trial methodologiesregulatory requirements
Soft Skills
communicationproblem-solving