Lead design, coordination and governance of the Hear Alert cohort trial, ensuring rigorous ethics, regulatory and protocol compliance.
Manage participant journey end-to-end, including recruitment, consent, training, support and retention across intraoperative and home settings.
Acquire, curate and quality-assure complex cochlear implant electrophysiology data, integrating intraoperative recordings with longitudinal home monitoring.
Contribute neurophysiological expertise to protocol refinement, biomarker interpretation, publications, conference presentations and industry-facing reports.
Provide operational leadership, mentoring students and staff, and fostering collaboration across academic, clinical and industry partners.

Hold a PhD or equivalent in audiology, neuroscience, biomedical science, biomedical engineering or a closely related clinical discipline.
Demonstrate substantial experience conducting human clinical studies, including ethics submissions, consent processes, recruitment and longitudinal retention.
Bring hands-on expertise with clinical electrophysiology systems and feel comfortable working within operating theatre or procedural environments.
Show capability managing complex clinical datasets, including database design, data integrity checks and documentation for regulatory-grade research.
Collaborate effectively with surgeons, clinicians, engineers, industry partners and participants across multidisciplinary, multi-site trial environments.
Contribute peer-reviewed outputs and mentoring, and welcome opportunities to translate neurophysiology into clinically impactful hearing technologies.

Senior Clinical Research Scientist, Neurophysiologist

Key skills