Data Engineer for Clinical Trials 80 - 100 % (f/m/d)

How you can make a difference :

Join our Clinical Research and Innovation team and contribute to clinical trials that shape the future of mechanical ventilation technology. As a Data Engineer for Clinical Trials, you will play a key role in developing and maintaining data management tools, analyzing clinical study data, and collaborating with medical experts to generate valuable research insights and scientific publications.

Your Responsibilities

• Design, development, testing and validation of clinical study data bases

• Implementation of data management tools for automating data cleaning and pre-processing pipelines, including data transfer, storage, conversion, anonymization, quality validation, and filtering.

• Detect inefficiencies; optimize processes and data flows

• Work closely with clinical team members and medical experts on e.g. clinical trial protocol development, data management plan development, clinical study report writing.

• Develop, implement, and test electronic case report forms (eCRFs) to ensure accuracy and compliance.

• Conduct exploratory data analysis and assess pilot patient data.

• Perform software analyses of clinical study data to test research hypotheses for study reports and publications.

• Provide technical support to clinical collaboration partners regarding ventilator data recording tools.

That's what you bring along :

• Master's degree in a relevant engineering or scientific field (e.g., Software Engineering, Biomedical Engineering, Electronics, Physics, Statistics, or related disciplines).

• Strong programming skills in Matlab and Python (experience in C++, C#, or C is a plus).

• At least two years of clinical database development experience including hands-on experience with large-scale database management.

• Passion for clinical research and an interest in contributing to scientific publications.

Experience and knowledge in the following areas are also an advantage:

• Knowledge of clinical trial regulations (e.g., ISO 14155, GCP, MDR, FDA) and regulatory requirements for clinical data management incl. data protection regulations (GDPR, HIPAA).

• Experience in software specification and validation (computer system validation).

• Good knowledge of data engineering concepts (Data Lake, Data Warehouse, etc.)

• Familiarity with electronic Case Report Form (eCRF) development, programming, and testing.

• Background in statistical analysis and data interpretation for clinical research.

Learn more about career opportunities at Hamilton at jobs.hamilton.ch .

Do you share our values and feel at home in a cooperative and down-to-earth environment? At Hamilton, we not only offer a motivating working environment, but also various leisure activities and modern working conditions. Our interactions at eye level encourage open communication and a pleasant working environment. Become part of a team where your skills are valued and innovative ideas are fostered. Interested? Then apply online using the "Apply now" button. If you have any questions, please contact us at Write an emailwith the following details:

Applications by post or e-mail can unfortunately not be considered.