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Job-Zusammenfassung
Das Department of Clinical Research (DCR) bietet vielfältige Möglichkeiten.
Aufgaben
Entwicklung und Pflege des DCR Qualitätsmanagementsystems.
Förderung einer Qualitätspolitik durch Verfahren und Prozesse.
Überwachung von Audits, Schulungen und Qualitätsindikatoren.
Fähigkeiten
Hochschulabschluss in Naturwissenschaften oder verwandtem Bereich.
Erfahrung im Qualitätsmanagement klinischer Forschung.
Starke Kommunikations- und Teamarbeitsfähigkeiten.
Ist das hilfreich?
Department of Clinical Research Employment upon agreement, at the earliest opportunity. 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 consisting of a strong Research Unit, the Clinical Trial Unit (CTU), the Clinical Investigation Unit (CIU), and one new subunit in 2025 - Medical Data Science (MDS) - and a planned Gender Medicine Unit (GM). DCR is a diverse department that provides expertise, innovation, leadership, contemporary pedagogy, and centralized facilities for supporting clinical researchers. DCR offers clinical researchers full support from study design to study implementation. DCR works across multiple collaborations with the Medical Faculty of the University of Bern and the University Hospitals. We are looking for a dedicated and detail-oriented Quality Manager to ensure our clinical research meets high standards and complies with ISO 9001 and all relevant regulations.
Tasks
Maintain and further develop the DCR Quality Management System in alignment with applicable regulatory and organizational requirements
Promote a culture of quality by implementing and supporting quality-related policies, procedures, and processes
Create, review, and approve controlled quality documents (Manuals, SOPs, etc.)
Oversee and support key quality processes, including:
Internal audits and vendor qualification
Risk and change management
Document control and archiving
Error and CAPA management
Training and quality reviews
Act as quality delegate during audits, inspections, and ISO 9001 (re)certification
Ensure all staff are trained on quality systems and GCP requirements
Monitor and report key quality indicators and manage customer feedback and complaints
Ensure computerized systems are validated, compliant, and fit for purpose across their lifecycle
Requirements
University degree (or equivalent) in natural sciences or a related field
Experience in quality management for patient-oriented clinical research
Solid knowledge of GCP, Human Research Act, Data Protection Law, and ISO 9001
Strong skills in documentation, record keeping, and attention to detail
Project leadership abilities with a positive and motivating attitude
Strong coordination and collaboration skills; able to work independently and as part of a team
Confident communicator with a diplomatic, proactive, and goal-oriented mindset
Fluent in English an German (written and spoken); other languages are a plus
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 (up to 50% of the time).
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.
Contact
If you have any inquiries, please contact Dr. Ueli Reber, Director CTU operations a.i. & Head of Business Operations, (Tel. +41 31 684 68 31, Email: E-Mail schreiben).
Are you interested? Then please send us your online application to HR Administration (E-Mail schreiben) by (15th July 2025), at the latest.