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Clinical Research Associate
Experience in clinical patient management
Sobre nosso cliente
Is a global, full-service Clinical Research Organization (CRO) specializing in a multitude of therapeutic areas.
Descrição do cargo
- Conduct qualification, initiation, monitoring, and closeout visits for research sites according to Medpace/Sponsor SOPs and GCP;
- Maintain ongoing site correspondence and site files;
- Complete visit reports and maintain study-related databases;
- Oversight and interaction with clinical research sites; and
- Review of patient charts and clinical research data.
- University degree in health-related field;
- Experience as CRA;
- Proven track record of demonstrating experience in clinical patient management, protocol, CRF, preparing of ISF, documentation to be submitted to competent authorities;
- Computer literacy;
- Excellent verbal and written communication skills in local language and English.
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