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Die UniBE ist renommiert.
Bei uns profitieren Sie vom guten Ruf einer traditionsreichen Institution in der ganzen Welt.
Clinical Study Manager 80-100%
Arbeitsbeginn
oder nach Vereinbarung
Arbeitsverhältnis
befristet
Institut / Arbeitsort
The Department of Clinical Research (DCR)
The Department of Clinical Research (DCR) is an academic center and umbrella organization supporting clinical researchers at the University of Bern and the University Hospitals. It is comprised of a range of established academic research units, dedicated methodological divisions, a Clinical Investigation Unit, a Medical Data Science subunit established in 2025, and a Gender Medicine Unit scheduled for implementation in 2026.
The DCR is a multidisciplinary institution that serves as a central body for expertise, innovation, strategic leadership, modern pedagogical approaches, and integrated infrastructure to support clinical research. It offers support to clinical researchers, along the entire research process from study design to implementation. DCR maintains close collaborative ties with the Medical Faculty of the University of Bern and the associated University Hospitals.
The DCR is a national leader in Switzerland in the field of Patient and Public Involvement (PPI), which refers to the active involvement of patients and members of the public in the design, conduct, and dissemination of research. PPI helps ensure that research is relevant, transparent, and aligned with the needs and priorities of those it aims to benefit.
We are looking for a Clinical Study Manager at the DCR to start in 2027. This is a fixed-term position for an initial period of 3 years with possibility of renewal, in accordance with the University of Bern's employment regulations.
Your qualifications and skills
*Apply strong project management skills to plan, coordinate and drive complex clinical research projects, ensuring timelines, deliverables and milestones are met.
*Proactively identify challenges, take initiative and drive solutions in collaboration with internal and external stakeholders.
*Contribute to protocol development and budget planning, ensuring regulatory compliance and operational feasibility.
*Coordinate and contribute to site feasibility assessments and site selection with investigators and relevant stakeholders
*Lead and coordinate study start-up, site activation and close-out independently.
*Prepare and submit ethics and regulatory applications, amendments, safety reports and notifications.
*Contribute to CRF/eCRF design and data management planning.
*Train study teams in line with protocol, SOPs and ICH-GCP.
*Manage study contracts and budgets.
*Prepare, review and quality-check essential documents and maintain the Trial Master File for inspection readiness.
*Coordinate stakeholders, including CEC, DSMB groups, and contribute to continuous improvement of processes.
*Vendor and CRO oversight.
Requirements
*Master's degree in a health or life science-related field; advanced degree or certificate in clinical trial management/coordination or regulatory affairs is an asset.
*At least 2 years relevant clinical studies experience, including demonstrated responsibility for independently managing studies or substantial study components.
*Solid knowledge of ICH-GCP and the clinical research regulations (HRA/ClinO); ISO 14155 / MDR a plus.
*Demonstrated ability to manage multiple projects in a clinical research environment.
*Financial management and budget oversight experience.
*Strong organizational, problem-solving, and risk management skills. Careful and systematic approach to administrative tasks.
*Excellent communication skills in English and German (written and oral).
*Ability to work independently while effectively coordinating cross-functional teams.
*Experience of working in academic research environment is an asset.
*Familiarity with clinical trial systems such as EDC, CDMS.
We offer
*An interesting and versatile role in a growing department, contributing to the successful development of the DCR.
*An international and dynamic environment with a motivated and diverse team, dedicated to high quality (research).
*A good work-life balance thanks to flexible working hours and the possibility of working from home.
*Opportunities for further training and programs within the University and a wide range of sports activities through 'Uni Sport'
*Salary and comprehensive social benefits according to cantonal guidelines.
Ihre Benefits
Internationales Renommee
Gute Forschungsinfrastrukturen und internationales Netzwerk
Kollaboratives Umfeld und ambitioniertes Team
Individueller Karrieresupport
Arbeiten an der UniBE
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