CLINICAL RESEARCH COORDINATOR
On-siteSingapore, Singapore
Job Summary
Conduct subject recruitment, scheduling, and data entry for multi-site Human Biomedical Research studies. Screen patients based on eligibility, obtain consent, administer questionnaires, and follow up on participants while communicating study aims in layman terms. Manage research documentation by collecting data from electronic health records, maintaining investigator files, and ensuring strict adherence to Good Clinical Practice and the Human Biomedical Research Act. Prepare audit documentation, coordinate IRB applications and amendments, and liaise with clinicians and laboratory teams to establish clinical workflows. Work Monday to Friday with Saturday coverage, requiring travel between hospitals and external sites.
Required Qualifications
- Bachelor Degree in Science/ Public Health/ Social Science
- 2 years relevant experience
- Able to adapt in a fast-paced environment
- Strong interpersonal and communication skills
- Leadership and accountability to tasks
- Independent and mature
- Able to work independently, as well as in a team
- Meticulous, well-organized and able to multi-task
- Ability to work in an interdisciplinary environment with different groups of stakeholders
- Willing to travel between the Hospitals and external study sites as part of his / her work
- Work Hours: Monday to Friday, 8:00AM to 4:30PM, and Saturday, 8:00AM to 12:30PM
- Knowledge of Good Clinical Practice (GCP) guidelines and the Human Biomedical Research Act (HBRA)
Desired Qualifications
- Strong focus to meet research deliverables and targets
Hiring someone like this?
Get your role in front of qualified candidates on Sorce.