Clinical Trial Manager Jobs in Basel
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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...
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C028 (FCRS = CH028) Novartis Pharma AG-Basel-appcast.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...
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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...
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F. Hoffmann-La Roche Gruppe-Basel-appcast.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...
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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, including...
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F. Hoffmann-La Roche AG-Basel-appcast.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...
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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...
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Coopers Group AG-Basel-
Excursion Management for clinical trials, including performing assessments and managing Expert Statements/Opinions.
• Support clinical studies by reviewing and approving IMP Supply & Release Flowcharts, Transfer requests, and Expert Opinions.
• Establish...
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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...
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Hays-Basel-
PTDS-L)
• Inspection Management: Actively drive and support all GxP inspections and audits
• Quality Decision-Making: Manage Temperature Excursion Management for clinical trials, including performing assessments and managing Expert Statements/Opinions...
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Roche-Basel-
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...
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Unilabs-Basel-
bypassing
standard procurement layers to engage directly with the clinical decision-makers feeling the pain of delayed
trials.
2. Complex Deal Execution
• Solution Architecture: Work with Pharma sponsors to define the exact diagnostic footprint required...
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Novartis Farmacéutica-Basel-
lead writing of scientific publications; present study results externally where appropriate.
Leadership: Lead study‑specific teams/clinical trial teams in partnership with other line functions. Lead BR‑sub‑team(s) on Global Project Teams for late‑phase...
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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...
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Gi Life Sciences Basel-Basel-
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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