Description:
- Coordinate study start-up activities
- Plan, organize and coordinate the workflow of the study
- Assisting with informed consent process by providing information to and educating research subjects, data collection and surveys
- Coordinate all relevant subject visits, ensuring minimum deviation from schedule of visits
- Monitor the quality of research ensuring compliance with the guidelines and standards
- Assist with all external monitoring, audit and inspection visits
- Monitor the financial aspects of the assigned study and advise the stakeholders accordingly
- Work with PI and department to respond to any audit findings and implement approved recommendations
- Assist with study closure activities including archival and assisting with all audits/ inspections/ monitoring
Requirements:
- Min. Degree in Science
- No exp needed, training provided
- Exp / internship in clinical research will be an advantage
Working hours: Mon - Fri, office hours
Location: Novena
Interested candidates, please forward your resume to [email protected]
Consultant: Huang Jingsheng Kevyn (R1333338)
Recruit Express Pte Ltd (99C4599)
