Job Description

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