- Coordinate study start-up activities, including assisting with feasibility reviews and furnishing of regulatory documents
- Plan, organize and coordinate the workflow of the study
- Development of materials and tools required for study start-up
- 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
- Assist PI to ensure timely amendments to study documents when required
- Monitor the quality of research ensuring compliance with HBRA, GCP, ICH & NHG guidelines and standards
- Conduct monitoring visits including Remote Monitoring and Site Monitoring
- 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
- Ensuring proper closure of study with all ethics and regulatory authorities
- Ensuring proper archiving of all study records including medical records, study documents, investigator files, subject files etc
Job requirements
- Min Degree in any science field
- Able to commence work within short notice
We regret that only shortlisted candidates will be contacted
Interested candidates please send your resume to [email protected]
Consultant: Tan Ming Hui, Michelle (Magdelene) (R21101623)
Recruit Express Pte Ltd (99C4599)
