Research Assistant / Clinical Research Associate
Gray Matter Solutions | Singapore
Gray Matter Solutions is a healthtech company focused on earlier detection and management of cognitive decline. We develop clinically validated digital tools for cognitive assessment and brain health, working with healthcare institutions, clinicians, researchers and industry partners across Singapore and internationally.
We are looking for a Research Assistant / Clinical Research Associate to support the execution of our clinical studies.
What You’ll Work On
Clinical Study Execution
- Coordinate and execute clinical research studies, including our ongoing industry-sponsored studies
- Support participant recruitment, screening, consenting, scheduling and follow-up
- Administer digital cognitive assessments and study procedures
- Coordinate with investigators, clinicians, research sites and external partners
- Maintain study documentation, participant logs and essential research records
- Support ethics submissions, amendments and regulatory/study documentation
- Ensure studies are conducted according to approved protocols and timelines
Data & Research
- Manage, clean and quality-check clinical research datasets
- Conduct basic statistical analyses and prepare study summaries
- Support interpretation of cognitive, clinical and biomarker data
- Assist with literature reviews and research synthesis
- Contribute to abstracts, posters, presentations and scientific manuscripts
Research Operations & New Studies
- Help design and operationalise new clinical and real‑world studies
- Support deployments with hospitals, clinics and community partners
- Develop research workflows, SOPs and data collection processes
- Identify operational bottlenecks and improve how studies are run
- Work across multiple projects as GMS expands its clinical evidence base
Who We’re Looking For
- Bachelor’s or Master’s degree in Psychology, Neuroscience, Biomedical Sciences, Life Sciences, Public Health or a related field
- Strong organisational skills and attention to detail
- Comfortable interacting with patients, research participants and clinicians
- Able to independently coordinate multiple moving parts and follow through reliably
- Comfortable working with clinical/research data
- Strong written and verbal communication skills
- Curious, resourceful and willing to learn quickly
Experience with any of the following would be advantageous:
- Clinical research or clinical trial coordination
- Cognitive or neuropsychological assessments
- REDCap or clinical research databases
- Statistical analysis using R, Python, SPSS or similar
- Ethics/IRB submissions
- Scientific writing or publications