Duties
- Coordinate study start-up activities, including assisting with feasibility reviews and furnishing of regulatory documents
- Plan, organize and coordinate the workflow of the study
- Coordinate all mandatory training requirements and documentation
- 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
- Ensure projects can be completed within the time frame and facilitate smooth running of research projects
- Monitor the quality of research ensuring compliance with HBRA, GCP, ICH & NHG guidelines and standards
- 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
- Ensuring proper closure of study with all ethics and regulatory authorities
Requirements
- Minimally diploma in biomedical science
- prior relevant experience in research will be an added advantage
Interested and qualified candidates, please send in your resume to [email protected]
Ivy Yong Shi Mei
R2198995
Recruit Express Pte Ltd 99C4599
