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Clinical Trial Manager Jobs in Basel

1 - 15 of 42
1 - 15 of 42
Search Results - Clinical Trial Manager Jobs in Basel
Manpower Basel-Basel
and compliance of clinical trial materials across the global supply chain. The team provides QA oversight for the global IMP Distribution Network and works closely with key stakeholders in Global Clinical Supply Chain Management Distribution. This position offers...
Proclinical-Basel
the clinical supply chain. In this role, you will develop and implement optimal clinical trial supply strategies, ensuring continuity of supply to patients while managing risks effectively. This position offers an opportunity to work on a diverse portfolio...
C028 (FCRS = CH028) Novartis Pharma AG-Basel
information. Please include the job requisition number in your message. Skills Desired  •  Clinical Research  •  Clinical Trials  •  People Management  •  Program Management  •  Regulatory Compliance  •  Resource Management (Organizational)  •  Risk Management #J-18808...
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Manpower Basel-Basel
Team: 7 people  •  Department: IMP Quality Distribution  •  Working hours: standard working hours Background IMP Quality Distribution is part of Global Quality Assurance and is responsible for maintaining the quality and compliance of clinical trial...
Coopers Group AG-Basel
are seeking a highly motivated and experienced Global Quality Manager to step into a role of significant reach. This position is instrumental in safeguarding product quality and regulatory compliance for global clinical trials. You will utilize your expertise...
ITech Consult AG-Basel
and changes for both internal procedures and external business documents (PTDS-L). Inspection Management: Actively drive and support all GxP inspections and audits. Quality Decision-Making: Manage Temperature Excursion Management for clinical trials, including...
F. Hoffmann-La Roche Gruppe-Basel
manager status  •  Closely interface with project team leaders as well as safety, clinical pharmacology, clinical operations, biostatistics, regulatory, research and biomarker groups and other members of project teams  •  Lead and/or support internal...
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ITech Consult AG-Basel
and changes for both internal procedures and external business documents (PTDS-L). Inspection Management: Actively drive and support all GxP inspections and audits. Quality Decision‑Making: Manage Temperature Excursion Management for clinical trials...
F. Hoffmann-La Roche AG-Basel
Scientists in a line‑ or functional‑manager capacity.  •  Interface closely with project team leaders and cross‑functional groups including safety, clinical pharmacology, clinical operations, biostatistics, regulatory, research, and biomarker teams.  •  Manage...
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Roche-Basel
functional teams on study analytics, data management, and safety profiles.  •  Scientific Leadership: Maintain the highest levels of scientific and clinical knowledge within the MS and Neuroimmunology therapeutic areas.  •  Regulatory Engagement: Take an active...
Universität Basel-Basel
provide all DBM researchers with access to a fully GMP-compliant environment for ATMP manufacturing and regulatory support for translational research projects and clinical trials. The GMP Facility for Advanced Therapies comprises two production sites...
Genentech-Basel
scalable and regulatory-ready innovations that enhance trial design, evidence generation, and clinical value of Roche medicines. The Opportunity The Expert Imaging Lead, Cardiovascular, Renal & Metabolism (CVRM) plays a pivotal role in advancing...
CTC-Basel
and maintain Company Core Data Sheet, labeling documents, risk communications, and Risk Management Plans  •  Review clinical trial materials (protocols, study reports, Investigator’s Brochure, ICF) to ensure alignment with safety strategies and risk management...
Novartis-Basel
IIa studies, working collaboratively with clinical, regulatory, biomarker, and profiling partners.  •  Leads the creation of clinical components of key documents e.g., Clinical Trial Protocols (CTPs), Investigator’s Brochures, Clinical Study Reports...
ITech Consult AG-Basel
and changes for both internal procedures and external business documents (PTDS-L).  •  Inspection Management: Actively drive and support all GxP inspections and audits.  •  Quality Decision-Making: Manage Temperature Excursion Management for clinical trials...
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