Clinical Trial Manager Jobs in Basel
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Search Results - Clinical Trial Manager Jobs in Basel
CTC Resourcing Solutions-Basel
of whom have given us some great feedback from their time working there.
Purpose
Participates in the planning and execution of one or more clinical trials or Expanded Access Programs including preparation of trial documents, management of Trial Master...
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...
appcast.io -
CTC Resourcing Solutions-Basel
CTC Resourcing Solutions is seeking an experienced Clinical Trials Manager for a 6-month maternity cover in Basel, Switzerland. The role involves planning, execution, and oversight of clinical trials, ensuring compliance with ICH-GCP standards...
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...
appcast.io -
Novartis-Basel
drug development process, Translational Medicine departments, clinical trial process, and the tools and technical platforms you’ll use.
Throughout the program, fellows reunite for continuous learning focused on soft skills, cross‑functional exposure...
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...
appcast.io -
Novartis-Basel
projects/products and actively participate in the Global Program Team (GPT), Global Clinical Team (GCT), and Clinical Trial Team (CTT). Lead the Safety Management Team (SMT). Responsible for managing safety issues from the formation of the GPT through Life...
Coopers Group AG-Basel
for the collection and delivery of clinical trial samples (e.g. Safety, Chemistry, Biomarker, PK and PD) across the portfolio of trials. The BOL is an integral part of the Clinical Trial Team and provides operational/ project management expertise as it relates...
stellen-basel.ch -
Elan Personal AG-Basel
to release pharmaceutical products for clinical trials, and finally for commercial supply. The QC-Section within the Analytical Development Department is responsible for the Release of Materials based on the GMP compliant execution of Analyses of Inprocess...
Revolution Medicines-Basel
across early‑ and late‑stage CMC regulatory activities, including clinical trial applications, initial marketing authorization applications (MAA), post‑approval variations, and lifecycle strategy.
The position requires deep expertise in EU regulatory...
Roche-Basel
the delivery of these roadmaps. This includes securing governance endorsement and resourcing; leading CoE matrix team delivery; managing vendor/technology partnerships; ensuring seamless integration of sensor-based DHTs into clinical trials, including study...
roche.com -
Novartis AG-Basel
projects/products and actively participate in the Global Program Team (GPT), Global Clinical Team (GCT), and Clinical Trial Team (CTT). Lead the Safety Management Team (SMT). Responsible for managing safety issues from the formation of the GPT through Life...
jobup.ch -
Work Selection AG-Basel
Chromatography (GC), Ion Chromatography (IC), Mass Spectrometry (MS), and others. The ultimate goal of our work is a robust control strategy to release pharmaceutical products for clinical trials, and finally for commercial supply.
The QC-Section within...
jobcourier.ch -
Basel
Coordinate the preparation, submission, management and maintenance of regulatory submissions related to clinical and non‑clinical development activities, including but not limited to:
• Clinical Trial Applications (CTAs)
• Submissions...
michaelpage.ch -
Basel
Overall accountability for drug supply chain in preclinical and clinical trials.
Qualifications:
• PhD or MSc in Organic or Analytical Chemistry, Pharmaceutical Chemistry, Pharmaceutical Sciences or related scientific discipline.
• Two (for PhD) or five...
icims.com -
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