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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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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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 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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Stiftung Weizenkorn-Basel
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.
Support clinical studies...
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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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Manpower Basel-Basel
and provide scientific input into study management, signal evaluation, benefit-risk assessments, regulatory submissions and risk management activities. The position requires a strong understanding of drug safety, clinical development and regulated GxP...
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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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Idorsia-Basel
while partnering closely with physicians, clinical teams, regulatory colleagues, and external partners to ensure compliance with global pharmacovigilance requirements.
Your Responsibilities:
Case Management & Safety Reporting
• Manage adverse event...
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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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Novartis Farmacéutica-Basel
Provide expert safety input to the clinical development program for assigned projects/products and be an active member of the Global Program Team (GPT), Global Clinical Team (GCT) and Clinical Trial Team (CTT) -Is responsible for safety issue management...
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Manpower Switzerland-Basel
to-end clinical trial lifecycle.
Proven experience with signal detection, risk management, aggregate reporting and safety documentation.
Ability to work independently with minimal supervision and strong self-leadership.
Strong analytical skills...
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Abbott Laboratories-Basel
to PSURs, clinical overviews, and risk management plans
• As part of the Labeling Sub‑Team, provide medical input and scientific strategies for global and national label changes, including safety‑related updates
• Ensure that all medical and promotional...
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Stiftung Weizenkorn-Basel
management activities including preparation and maintenance of CCDS, labeling document maintenance (including IB), risk communications, RMP.
Review of clinical protocols, study reports, Investigator's Brochure (IB), informed consent form (ICF) and other...
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Abbott Laboratories-Basel
Act as a core member of the Product Safety Team, overseeing medical safety monitoring and contributing to PSURs, clinical overviews, and risk‑management plans
• As part of the Labeling Sub‑Team, provide medical input and scientific strategies...
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