Clinical Data Architect & Trials Lead

Liechtenstein Business; Schweiz; Hybrid; EUR 116.000 - 158.000; Vollzeit

Zusammenfassung

Hamilton Medical is seeking a Medical Research Engineer to develop and maintain data management tools, analyze clinical study data, and collaborate with medical experts to publish research findings. You will handle data acquisition, quality checks, and analysis for trials in critical care contexts.

The role involves developing eCRFs and databases, coordinating across sites and CROs, and ensuring regulatory compliance. English proficiency is required; travel up to 10% is expected.

Qualifikationen

• Master's degree in a relevant engineering, scientific, biomedical, statistics, data science, or related field.
• Strong programming skills in MATLAB and Python (experience in C++, C#, or C is a plus).
• Experience with medical device data, physiological signals, or time-series data in clinical/research settings.

Aufgaben

• Implement data management tools and automated workflow for clinical and medical device data.
• Process and analyze medical device data, physiological signals, and time-series data.
• Conduct exploratory data analyses and software-based analyses of clinical study data.
• Develop, implement, test, and validate electronic case report forms (eCRFs) and clinical databases.
• Perform ongoing clinical data review, data cleaning, and reconciliation activities.
• Coordinate and support clinical studies across study lifecycle.
• Support clinical project planning, timelines, budgets, and risk management.
• Act as a key contact for investigators, sites, CROs, EDC providers, and internal teams.

Kenntnisse

MATLAB

Python

English fluency

German language (plus)

Ausbildung

Master's degree in engineering/science/biomedical/data science

Tools

PDMS

eCRF development tools

Jobbeschreibung

Hamilton Medical is seeking a Medical Research Engineer to develop and maintain data management tools, analyze clinical study data, and collaborate with medical experts to publish research findings. You will handle data acquisition, quality checks, and analysis for trials in critical care contexts.

The role involves developing eCRFs and databases, coordinating across sites and CROs, and ensuring regulatory compliance. English proficiency is required; travel up to 10% is expected.