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Clinical Trial Manager Jobs

1 - 15 of 139
1 - 15 of 139
Search Results - Clinical Trial Manager Jobs
Coopers Group GmbH-Basel
Contract Duration: 1 year/possible extension Location: Basel Responsibilities You will be responsible for supporting the overall clinical and scientific activities regarding study planning preparation, management, evaluation, monitoring...
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Coopers Group AG-Basel
Contract Duration 1 year / possible extension Location Basel Responsibilities You will be responsible for supporting the overall clinical and scientific activities regarding study planning preparation, management, evaluation, monitoring...
Syneos Health, Inc.-Schweiz
A leading biopharmaceutical solutions organization in Switzerland seeks a Global Trial Optimization Specialist to support clinical study planning and recruitment. Responsibilities include creating recruitment materials, managing recruitment vendors...
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Ironwood Pharmaceuticals-Basel
execution, and interpretation of clinical trials and the clinical development plan. You will work with the study management teams, training internal and external staff, monitoring clinical data, and responding to health authority requests related...
Ironwood Pharmaceuticals, Inc.-Basel
of clinical trials and the clinical development plan. You will work with the study management teams, training internal and external staff, monitoring clinical data, and responding to health authority requests related to the assigned clinical development...
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Coopers Group AG-Basel
and interpretation of clinical trials and the clinical development plan. You will work with the study management teams, train internal and external staff, monitor clinical data, and respond to health authority requests related to the assigned clinical development...
Global Antibiotic R&D Partnership (GARDP)-Geneva
strategy discussions where appropriate  •  Draft study design concepts/synopsis, protocols and amendments in collaboration with study operations lead/clinical trial manager, Associate Director Medical Sciences/Medical Lead, statisticians, and others where...
workable.com -

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Johnson & Johnson-Allschwil
A global healthcare leader is seeking an Innovation Leader in Allschwil, Switzerland, to design and execute innovative clinical trial projects. This role requires a Bachelor's degree and a Master's preferred, alongside a minimum of 4 years of work...
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Basel
field, or equivalent related education and experience, plus extensive experience in clinical research and commercialization.  •  Graduate degree (MBA/PhD/MD) is a plus.  •  Significant experience in the clinical trial industry, with deep knowledge...
stellen-basel.ch -
PowerToFly-Zug
of clinical trials.  •  Accountable for ensuring adherence to applicable global and local regulations, ICH Guidelines and AbbVie Quality Management System, promoting a quality driven local organization, oriented to continuous improvement and excellence...
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gloor&lang AG-Basel
Trial Materials management  •  Proven experience working with CDMOs (packaging, labeling, distribution)  •  Hands-on experience with RTSM/IRT platforms (e.g., IXRS, 4G Clinical, Cenduit, Medidata RTSM)  •  Solid understanding of clinical supply planning...
join.com -
GSK-Zug
requires a physician capable of developing and executing oncology clinical trials, supporting the successful clinical development, regulatory filing and initial market launch of a growing portfolio of innovative and transformational Oncology agents...
nemensis ag-Riehen
Recruit For  •  Marketing authorisation applications and regulatory submission management for pharmaceuticals and medical devices  •  Global regulatory strategy development across EU, US, and Swiss regulatory frameworks  •  Clinical trial authorisation...
1 similar job: Basel
Interim Legal AG-Zurich
management, and providing legal guidance on industry regulations. Ideal candidates should be fluent in English and have experience in clinical trial operations. A competitive salary and growth opportunities are provided, along with a commitment to diversity...
Rüti
at an investigator/physician site such as protocol deviation/violations and pharmacovigilance issues.  •  Per the Clinical Monitoring/Site Management Plan (CMP/SMP): Assesses site processes. Conducts Source Document Review of appropriate site source documents...
stellen-zuerich.ch -
2 similar jobs: Zürich, Wald
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