CLINICAL RESEARCH COORDINATOR

Job Category: Research
Posting Date: 28 Aug 2025
We are looking for a candidate who will be providing research support service to the investigators in the conduct and implementation of clinical trial and/or clinical research studies at the National Neuroscience Institute (SGH Campus), in adherence to Singapore Guideline for Good Clinical Practice (SGGCP) and protocol requirements.

These are some of the day to day duties:

• Perform study-related activities, such as screening and recruitment of study subjects; assist with obtaining informed consent; coordination of subject visits; and other procedures
• Administer study-related questionnaires
• Assist in data collection and data management
• Assist in all administrative requirements including submission process to IRB and/or regulatory authority
• Work closely with internal and external stakeholders to ensure all study-related activities are carried out efficiently

There will be opportunities to:

• Contribute to human biomedical research and/or clinical trials set-up, feasibility and coordination
• Contribute to data processing and analysis of results for multiple studies conducted within the department
• Acquire new skillsets, such as imaging handling, processing and analysis
• Gain experience in scientific writing for presentations and publications

Requirements:

• Bachelor’s degree in Life Sciences, Psychology or related fields
• Good communications and interpersonal skillsStrong attention to detail
• Excellent organisational skills and ability to manage multiple priorities
• Good IT literacy and statistics skills are also desirable
• Prior experience in a clinical environment and/or with clinical trials/studies would be most advantageous
• Prior experience in phlebotomy will be an advantage

Req ID: 3193

• Perform study-related activities, such as screening and recruitment of study subjects; assist with obtaining informed consent; coordination of subject visits; and other procedures
• Administer study-related questionnaires
• Assist in data collection and data management
• Assist in all administrative requirements including submission process to IRB and/or regulatory authority
• Work closely with internal and external stakeholders to ensure all study-related activities are carried out efficientl