Clinical Trial Manager Jobs in Allschwil
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Search Results - Clinical Trial Manager Jobs in Allschwil
Witzig The Office Company AG-Allschwil
The Clinical Supply Manager is accountable for management, coordination and efficient on-time delivery of trial supplies (including IMP= Investigational Medicinal Product, Placebo, Standard of Care and clinical ancillaries) for global clinical...
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Witzig The Office Company AG-Allschwil
Witzig The Office Company AG is looking for a Clinical Supply Manager in Allschwil, Switzerland, to manage the supply of trial materials for global clinical studies. The role includes coordinating demand forecasts, overseeing documentation...
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Idorsia Pharmaceuticals Ltd-Allschwil
development and delivery of clinical sections of trial- and program-level regulatory documents, including Investigator’s Brochures, briefing books, safety updates, submission dossiers and responses to Health Authorities.
• Provide thought leadership...
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Alentis Therapeutics-Allschwil
management:
• Develop demand forecasts and supply plans based on study protocols, clinical scenarios and enrollment projections.
• Plan, implement and execute the supply strategy for trial medication and ancillary supplies in collaboration with clinical...
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8542-Actelion Pharmaceuticals Ltd Legal Entity-Allschwil
and helps with the clinical development plan, the development of the clinical trial protocol, clinical trial materials including protocol training, content of clinical study reports and relevant documents for regulatory filings.
The SRP provides critical...
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Idorsia Pharmaceuticals Ltd-Allschwil
Manager (Artwork Focus) to join our Commercial Packaging & Clinical Trial Supply Team !
Job Responsibilities
• Lead and manage commercial pharmaceutical artwork projects across the product lifecycle, ensuring timely delivery, quality, compliance...
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Jobtailor-Allschwil
ongoing safety review, and medically relevant vendor and operational deliverables.
• Works cross-functionally with Clinical Operations, Regulatory, Biostatistics, Data Management, Drug Safety, Clinical Pharmacology, Translational Medicine, Medical Writing...
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6010-Biosense Webster Inc. Legal Entity-Allschwil
Providing regulatory oversight for clinical trial‑related device labeling and documentation, including Instructions for Use (IFU), investigator materials, and associated records.
• Ensuring compliance with applicable global device regulations and standards...
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Proclinical Group-Basel, 3 km from Allschwil
and data interpretation.
• Prepare and lead dose escalation meetings with investigators and ensure real-time availability of quality clinical trial data.
• Proactively lead risk mitigation discussions and implement risk management strategies at the trial...
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Proclinical Group-Basel, 3 km from Allschwil
to the design, execution, and oversight of global clinical studies, primarily focusing on low-complexity trials. This role involves close collaboration with cross-functional teams to ensure study deliverables are met while maintaining high scientific...
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