Our client is expanding their clinical operations team and is looking for a Clinical Research Associate / Clinical Operations Associate to support the planning and execution of ongoing and upcoming clinical studies. The head office is based in the United States, with a Singapore clinical research branch established in the western region of Singapore.
Key Responsibilities :
- Support day-to-day management and execution of clinical trials in Singapore
- Conduct and document site monitoring visits(pre-study, initiation, routine, and close-out)
- Assist in the development of trial protocols, CRFs, and related study documentation
- Coordinate ethics submissions and regulatory applications (IRB / HSA)
- Track investigational product and trial materials to ensure compliance with GCP and SOPs
- Provide project management support - tracking timelines, vendors, and procurement activities
- Collaborate closely with internal scientists, regulatory staff, and external clinical partners
- Oversaw coordination of project extensions with the CRO, facilitating communication between the Singapore and US headquarters, research centres, hospitals and pharmaceutical stakeholders
Requirements :
Bachelor's degree in Life Sciences, Medical Sciences, or related field2-5 years of experience in clinical research, clinical operations, or trial coordinationPractical experience in site monitoringand strong understanding of ICH-GCPOrganized, meticulous, and proactive with excellent documentation habitsClear communicator with the ability to work independently in a small, agile teamExposure to project or program management is a plusWhy Join Us
Be part of a mission-driven biotech tackling rare diseases from SingaporeWork in a hands-on, cross-functional environment where your contributions matterCompetitive salary and benefits packageGrowth opportunities into clinical operations, project management, or regulatory pathways