Responsibilities

• Conduct pre-study, initiation, monitoring, and closeout visits for research sites according to Company/Sponsor SOPs and GCP;
• Maintain ongoing site correspondence and site files;
• Complete visit reports and maintaining study-related databases;
• Oversight and interaction with clinical research sites; and
• Review of patient charts and clinical research data.

Qualifications

• University degree in health-related field;
• 2- 4 years of monitoring experience gained from a global CRO and /or other related clinical research environment is preferred;
• Proven track record of demonstrating experience in clinical patient management, protocol, CRF, preparing of ISF, documentation to be submitted to competent authorities, project management;
• Computer literacy;
• Should be both a team worker and self-motivated professional;
• Detailed-minded & well-organized;
• Strong determination to grow with the organization.

Song Zhao Hui EA License No. 02C3423 Personnel Registration No. R1761205

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