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 field
• 2-5 years of experience in clinical research, clinical operations, or trial coordination
• Practical experience in site monitoringand strong understanding of ICH-GCP
• Organized, meticulous, and proactive with excellent documentation habits
• Clear communicator with the ability to work independently in a small, agile team
• Exposure to project or program management is a plus

Why Join Us

• Be part of a mission-driven biotech tackling rare diseases from Singapore
• Work in a hands-on, cross-functional environment where your contributions matter
• Competitive salary and benefits package
• Growth opportunities into clinical operations, project management, or regulatory pathways