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Clinical Trial Manager Jobs

1 - 15 of 57
1 - 15 of 57
Search Results - Clinical Trial Manager Jobs
Roche Holding AG-Basel
in the pharmaceutical/healthcare industry and drug development (therapeutic area a plus), alongside a solid understanding of the clinical trial environment, ICH‑GCP, and lifecycle sequence/interdependencies.  •  You are highly experienced in clinical trial management...
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AXEPTA SA-Geneva
of evidence: IFU, risk management files, PMS data, trials and tests, labelling, complaints, vigilance and scientific literature.  •  Ensure the alignment of clinical data within all regulatory documentation.  •  Train and support the external providers involved...
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BeiGene, Ltd.-Basel
in fighting cancer. Position Regional Clinical Compliance (RCC) Inspection Manager is responsible for driving proactive risk management, sustained inspection readiness, audit support, and regulatory compliance across clinical trials. The role provides...
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SJP Biotec GmbH-Zurich
development field - RAS/eIF4A/translation-pathway inhibition. Key Responsibilities Translate and deliver key directives from the board and senior management, and serve as the clinical face of the company. Lead and manage all clinical development activities...
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BeiGene, Ltd.-Basel
BeOne is seeking a Regional Clinical Compliance (RCC) Inspection Manager to lead proactive inspection readiness and audit support across regional and global levels. You will guide clinical teams on inspection expectations, coordinate responses...
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SJP Biotec GmbH-Zurich
Key Responsibilities  •  Translate and deliver key directives from the board and senior management, and serve as the clinical face of the company.  •  Lead and manage all clinical development activities across the SJP portfolio  •  Design Phase 2 and 3...
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AXEPTA SA-Geneva
IFU, risk management files, PMS data, trials and tests, labelling, complaints, vigilance and scientific literature. Ensure the alignment of clinical data within all regulatory documentation. Train and support the external providers involved in drafting...
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Neurocrine Biosciences-Allschwil
to multidisciplinary project teams for assigned TA/Program, advises Senior Technical Leadership and Executive Management and regularly interfaces with internal and external colleagues to ensure timely and accurate dissemination of Clinical Pharmacology findings. Your...
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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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Rivia SA-Zurich
About Rivia Rivia is a data engine for clinical trial intelligence. It provides data infrastructure and AI-driven workflows for clinical trial teams, enabling biotechs to run studies more efficiently and to demonstrate which patients derive...
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Roche-Basel
understanding of the clinical trial environment, ICH-GCP, and lifecycle sequence/interdependencies.  •  You are highly experienced in clinical trial management tools, systems, and their interdependencies, specifically including IxRS, eCOA, centralised endpoint...
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roche.com -
Swiss Cancer Institute-Bern
research for a cure tomorrow," we conduct oncology clinical trials and serve as a key partner for authorities, professional associations, and the pharmaceutical industry. Approximately 70 employees at our Competence Center in Bern work closely with all...
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Debiopharm-Lausanne
Mission The Clinical Development Quality Manager (CDQM) is responsible for ensuring quality oversight across clinical development activities and supporting the maintenance of GCP compliance. This role supports stakeholders in vendor qualification...
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Debiopharm-Lausanne
is preferred;  •  At least 3 years of regulatory affairs experience in the field of drug development, including experience in managing clinical trials;  •  Demonstrated understanding of regulatory procedures in the EU and/or US;  •  Necessary skills...
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workable.com -
Neurocrine Biosciences-Allschwil
needs. The role requires extensive experience in drug development, regulatory strategy, and trial design, with a track record guiding projects through global regulatory submissions and risk management. #J-18808-Ljbffr...
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