Senior Clinical Research Associate – FSP
Parexel
full-time
Posted on:
Location Type: Remote
Location: Brazil
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Job Level
Tech Stack
About the role
- Responsible for site management, monitoring, and close-out of assigned clinical trials investigator sites
- Ensure patient safety and quality study execution in accordance with applicable laws, GCP, and client standards
- Manage investigator site relationships to ensure effective delivery of clinical trials
- Resolution of all protocol-related issues for assigned investigator sites
- Conduct onsite, remote/electronic monitoring as needed and ensure compliance with protocol
Requirements
- +3 years of monitoring experience
- Extensive knowledge of clinical trial methodologies
- Knowledge of ICH/GCP, FDA, and local regulations
- Bachelor's degree in life sciences or professional degree in life sciences such as nursing, pharmacy, medical background or equivalent
- Must be fluent in English and in the native language(s) of the country they will work in
Benefits
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Applicant Tracking System Keywords
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Hard Skills & Tools
clinical trial methodologiesmonitoring experienceprotocol complianceinvestigator site management
Soft Skills
patient safetyrelationship managementissue resolutioncommunication
Certifications
Bachelor's degree in life sciencesprofessional degree in life sciences