Clinical Data Analyst
Paris, France
Science is a clinical stage, vertically integrated technology company focused on solving some of neuroscience’s hardest questions and most serious unmet medical needs. We work to restore quality of life to those with debilitating conditions for which there are no treatment options, creating devices aimed at restoring vision, cognition, and mobility to patients who have lost it. To support progress across our industry, we provide state-of-the-art components and vertically integrated infrastructure for others to build on via Science Foundry.
We are seeking a strongly motivated Junior Clinical Data Analyst to join our team. This position combines rigorous data management and statistical analysis with hands-on involvement at our clinical sites. The successful candidate will support clinical data analysis and the creation of procedures related to develop and maintain data visualization tools and reports.The ideal candidate brings a strong foundation on statistics, an interest in medical devices or ophthalmology, and the adaptability to thrive in both office and clinical environments.
Role responsibilities:
- Collect, clean, and quality-control clinical data across multiple international sites using the eCRF platform, identifying and reporting discrepancies and protocol deviations
- Perform statistical analyses including psychophysical data processing (threshold estimation, staircase/reversal analysis), visual acuity metrics (logMAR, ETDRS), and patient outcome measures
- Develop and maintain data visualization tools and reports (R, Python) to support study monitoring, regulatory submissions, and scientific publications
- Assist in preparing Statistical Analysis Plans (SAPs) and contribute to regulatory documentation in compliance with ISO 14155, EU MDR 2017/745, ICH E6, and TGA requirements
- Collaborate with the Clinical Research Scientist and biostatistician on exploratory and confirmatory analyses for interim reports and manuscripts
- Support implementation and validation of clinical assessment software, including stimulus presentation tools
- Travel to clinical sites to support psychophysical testing sessions, assist during patient visits as a non-medical observer, and contribute to data collection procedures
- Provide on-site training and guidance to site staff on data entry protocols, eCRF use, assessment procedures, and PRIMA product-specific requirements
- Prepare and provision documents to support regulatory submissions
Key qualifications:
- Master's degree in biostatistics, biomedical engineering, data science, neuroscience, or a related quantitative field
- Proficiency in R and/or Python for data analysis and visualization
- Strong understanding of statistical methods (descriptive statistics, regression, confidence intervals, non-parametric tests)
- Excellent organizational skills and attention to detail
- Ability to communicate clearly in English and French, Italian or German are also encouraged
- Willingness and ability to travel up to 30% of working time
Preferred qualifications:
- Experience with data analysis methods
- Familiarity with psychophysical methods or sensory testing paradigms
- Live locally near our office in Paris