Central
12 months contract
Pre-Study
1. Coordinate study start-up activities, including assisting with feasibility reviews and furnishing of regulatory documents
2. Plan, organize and coordinate the workflow of the study
3. Development of materials and tools required for study start-up
4. Coordinate all mandatory training requirements and documentation
Study Recruitment and Conduct
1. Assisting with informed consent process by providing information to and educating research subjects, data collection and surveys
2. Coordinate all relevant subject visits, ensuring minimum deviation from schedule of visits
3. Ensure projects can be completed within the time frame and facilitate smooth running of research projects
4. Assist PI to ensure timely amendments to study documents when required
Study Monitoring, Audit and Inspection
1. Monitor the quality of research ensuring compliance with HBRA, GCP, ICH & NHG guidelines and standards
2. Conduct monitoring visits including Remote Monitoring and Site Monitoring
3. Assist with all external monitoring, audit and inspection visits
4. Monitor the financial aspects of the assigned study and advise the stakeholders accordingly
5. Work with PI and department to respond to any audit findings and implement approved recommendations
Study Closure
1. Assist with study closure activities including archival and assisting with all audits/ inspections/ monitoring
2. Ensuring proper closure of study with all ethics and regulatory authorities
3. Ensuring proper archiving of all study records including medical records, study documents, investigator files, subject files etc
How to Apply: send your resume and indicate role(s) you want to apply to: [email protected] or telegram @jocelynchan
Jocelyn Chan| Consultant | Recruit Express Pte Ltd (Healthcare & Lifescience) Company EA License number : 99C4599 Personnel EA License: R1331820
