Freelance Senior Clinical Research Associate – Georgian Speaking
ProPharma
part-time
Posted on:
Location Type: Hybrid
Location: Bucharest • Romania
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Job Level
About the role
- Responsible for conduct of all types of monitoring, and co-monitoring visits
- Responsible for monitoring report writing and completion
- Support development of study specific documentation
- Review and oversee regulatory documentations for accuracy and completeness
- Communicate with assigned clinical sites, investigators, and client personnel
Requirements
- > 5 years of experience as a Clinical Research Associate
- Excellent verbal and written communication skills
- Excellent computer skills with experience using Microsoft Office
- Electronic data capture (EDC) experience
- Knowledge of applicable local law, local regulatory requirements, ICH Guidelines, and GCPs
Benefits
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Applicant Tracking System Keywords
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Hard Skills & Tools
monitoringmonitoring report writingregulatory documentation reviewstudy specific documentation developmentelectronic data capture (EDC)GCP
Soft Skills
verbal communicationwritten communication