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Clinical Trial Manager Jobs in Basel

1 - 15 of 66
1 - 15 of 66
Search Results - Clinical Trial Manager Jobs in Basel
Pharmiweb-Basel
We are seeking an experienced and highly organized Clinical Trial Supply Manager to oversee the management and execution of clinical trial supplies from setup through to closeout. This role involves coordinating the timely delivery, packaging...
headcount AG-Basel
Clinical Trial Liaison Manager Location: Basel Contract: 12-month contract Start Date: ASAP Workload: Full-time Overview: Our client, a global pharmaceutical company, is looking for a Clinical Trial Liaison Manager (CTLM). This role is focused...
CK Group-Basel
Job Title: Commercial Packaging and Clinical Trial Supplies Manager Work Location: Allschwil, Basel Country: Switzerland Duration: 12 months Rate: Annual salary depending on experience Your main duties as an Commercial Packaging Manager...
WillHire-Basel
of clinical finished goods (supply drugs) to patients.  •  Study managers provide inputs in clinical study protocol, understand study design and are responsible for optimal clinical trial supply strategy in terms of packaging design, proactive planning following...
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TN Switzerland-Basel
with regulators of every country in which Roche does business to help them understand our products’ clinical value. We also work across industry and regulators to continually evolve regulatory policy. As a Clinical Trial Regulatory Lead (CTRL), you will lead...
Hobson Prior International Ltd-Basel
Hobson Prior is seeking a Commercial Packaging and Clinical Trial Supplies Manager for a contract role in Basel. This position focuses on managing the supply chain for clinical trials, ensuring timely delivery and compliance with regulations. You...
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TN Switzerland-Basel
Clinical Trial team.   4.  Advise on optimal clinical trial supply strategies, including packaging design and risk management.   5.  Review clinical trial protocols and develop packaging and supply designs.   6.  Maintain accurate clinical supply demand aligned...
C028 (FCRS = CH028) Novartis Pharma AG-Basel
Clinical Research  •  Clinical Trials  •  Clinical Trials Monitoring  •  Data Management  •  Health Sciences  •  Life Science  •  Project Management About Us Our purpose is to reimagine medicine to improve and extend people's lives. We use innovative science...
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headcount AG-Basel
the design, implementation, and management of clinical development plans _Collaborate with internal and external stakeholders to optimize trial designs and study protocols. _Provide medical expertise and oversight throughout all stages of clinical...
Healthcare Businesswomen’s Association-Basel
of GCP, clinical trial design, statistics, and regulatory and clinical development processes.   8.  Previous global people management experience is preferred, though this may include management in a matrix environment.  •  Final job title and associated...
DSM-Basel
Clinical Trial Management and Central Trial Oversight services provide for the regional / global coordination of clinical trial management activities for internally managed and / or outsourced trials. These services lead the Study Management Team...
Novartis Farmacéutica-Basel
Determine appropriate safety monitoring and risk management strategies.  •  Ensure compliance with all applicable regulatory and ethical guidelines.  •  Contribute to the preparation and submission of regulatory documents.  •  Analyze and interpret clinical trial...
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Acadia Pharmaceuticals Inc.-Basel
Clinical Trial Management and Central Trial Oversight services provide for the regional / global coordination of clinical trial management activities for internally managed and / or outsourced trials. These services lead the Study Management Team...
Novartis Farmacéutica-Basel
scientific partnerships with key stakeholders.   7.  Working knowledge of GCP, clinical trial design, statistics, and regulatory and clinical development processes.   8.  Previous global people management experience is preferred, though this may include management...
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BeiGene-Basel
execution, and oversight of vendor management and GCP audit activities to ensure compliance with GCP regulations. This role ensures that clinical trials and all vendors adhere to internal quality standards, regulatory requirements, and contractual...
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