What You’ll Work OnClinical 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
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