Clinical Trial Manager Jobs in Basel
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Search Results - Clinical Trial Manager Jobs in Basel
Manpower BaselBasel
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...
ProclinicalBasel
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 AGBaselappcast.io
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...
Manpower BaselBasel
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 AGBasel
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 AGBasel
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 GruppeBaselappcast.io
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...
RocheBasel
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...
F. Hoffmann-La Roche AGBaselappcast.io
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...
GenentechBasel
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...
Universität BaselBasel
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...
RocheBasel
development plans from Phase 1 through Phase 2 (proof-of-concept)
• Coach Clinical Scientists in a line- or functional-manager status
• Closely interface with project team leaders as well as safety, clinical pharmacology, clinical operations, biostatistics...
CTCBasel
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...
ITech Consult AGBasel
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...
Gi Life Sciences BaselBasel
assessments and third-party evaluation review.
Own quality documentation & change control (internal procedures + PTDS?L business documents).
Drive inspection/audit readiness and manage temperature excursion assessments for clinical trials.
Enable clinical...
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