Department of Clinical Research
Employment upon agreement
The is an environment for high-quality, future-oriented research. Strong connections between basic research, engineering sciences, and university hospitals enable a unique setting for translational and patient-centered clinical research. The faculty prioritizes cross-disciplinary research and, fostering innovation in medical science. It is one of the largest medical faculties in Switzerland and is affiliated with the country's largest hospital complex.
The Department of Clinical Research (DCR) is a joint initiative of the University of Bern's Faculty of Medicine and its university hospitals, including Inselspital and the University Psychiatric Services (UPD). It supports and professionalizes clinical and translational research collaborations. Our specialized divisions assist researchers throughout the entire research process, from project conception to result dissemination. We provide tailored educational programs and events on all aspects of clinical research, equipping researchers and students with the skills to conduct efficient and impactful studies. Our mission prioritizes patient-centered research, ensuring that patient perspectives are integral to our work.
We are establishing a new team to provide clinical researchers access to trial-quality real-world data (RWD) grounded in transparent, evidence-based validation. This includes conducting outcome validation studies for claims-based and EHR-based algorithms, such as disease and disease-severity phenotyping based on the Inselspital's EPIC data. This new RWD support team will pave the way for using RWD for clinical trials embedded in routine care, generating timely, randomized real-world evidence. It will work closely with the Pragmatic Evidence Lab (Prof. Lars Hemkens) and the Medical Data Science Unit (Prof. Benjamin Ineichen) at DCR.
Key challenges and opportunities
1. Developing innovative, evidence-based methods to make RWD trial-ready.
2. Integrating RWD into conventional clinical trial databases.
3. Evaluating the reliability of RWD for trials,. testing where EPIC-based RWD can replace manual adverse event assessments.
4. Systematically assessing the validity of trial outcomes derived from routine data through empirical research, validation studies, and meta-research.
5. Defining how to make best use of health data for patient-centered, pragmatic research.
This role is central to transforming how research is embedded in routine care at the University of Bern and its university hospitals. It is a key role integrating research across various groups within DCR, particularly the Segelov research lab, the STRIDE lab (led by Prof. Benjamin Ineichen, Professor of Medical Data Science) and the Pragmatic Research Lab (led by Prof. Lars Hemkens, Academic Director of Clinical Trials at DCR). Please review the DCR and research groups on .
Your Role
As a Postdoctoral Researcher, you will play a central role in this initiative by:
1.Contributing to the conceptualization, setup, and implementation of a state-of-the-art RWD team at DCR.
2.Developing innovative methods and frameworks to assess and measure data-quality from the perspective of clinical trial applications.
3.Conducting meta-research and validation studies for outcome and/or phenotyping algorithms using routine data.
4.Co-designing research protocols, data pipelines, and governance frameworks for RWD-based phenotyping.
5.Adapting and translating established models of EPIC/EHR use from other institutions to the University of Bern.
6.Supporting protocol design for randomized trials, ensuring regulatory compliance and methodological rigor from a data perspective.
7.Collaborating with clinical researchers, data scientists, and international partners to embed research into care.
8.Contributing to grant writing and fundraising efforts to ensure sustainability of the academic team.
9.Training and mentoring junior researchers and students in RWD and validation methods.
10.Disseminating findings through high-impact publications and conference presentations.
Your Profile
6. MD and/or PhD in clinical research (epidemiology, biostatistics, or a related field will be considered also).
7. Hands-on experience in medical data science/biomedical informatics.
8. Hands-on experience with clinical trial design, conduct, and/or analysis, supported by a publication record.
9. Experience in working with RWD and/or validation or meta-research, supported by a publication record
10. Advanced programming and data management skills, including data engineering (. Python, R, SQL; EPIC/Caboodle experience is a plus).
11. Ability to efficiently work independently under tight deadlines with general guidance in multidisciplinary teams.
12. Ability to prepare manuscripts, grant proposals, and scientific meeting presentations
13. Fluency in English (German is an asset).
We offer
14. An academic role at the intersection of data science, clinical research, and advanced trial methodology, with real impact on patient-centered evidence generation.
15. The opportunity to help establish a new RWD support team at DCR Bern, directly enabling research that is embedded in care.
16. A supportive academic environment with opportunities for career development, mentoring, publications, and independence.
17. A strong commitment to open science and publication in peer-reviewed scientific articles.
18. Access to a dynamic machine learning community at the University of Bern, with a strong emphasis on digitalization ().
19. Integration in a wide network of clinical researchers and meta-researchers locally, nationally and internationally.
20. Collaboration within Switzerland's largest medical faculty and hospital complex, offering extensive networking opportunities.
21. Competitive employment conditions under University of Bern regulations.
Contact
Before applying, we strongly recommend you discuss the position and your suitability with Prof. Eva Segelov