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Clinical Trial Manager Jobs

1 - 15 of 44
1 - 15 of 44
Search Results - Clinical Trial Manager Jobs
Octapharma AG-Lachen
Clinical Trial Manager - Central Monitoring Become part of a vital chain and contribute to our common goal of making people’s lives better. Headquartered in Lachen, Switzerland, Octapharma is one of the largest human protein manufacturers...
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BeiGene, Ltd.-Basel
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 agreements, thereby supporting...
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Octapharma AG-Lachen
Clinical Trial Manager - Central Monitoring Become part of a vital chain and contribute to our common goal of making people’s lives better. Headquartered in Lachen, Switzerland, Octapharma is one of the largest human protein manufacturers...
Read more
Universitätsspital Zürich USZ-Zurich
against validation frameworks  •  Support the implementation of ISO 9241-210-conformant usability studies (dashboards, ePRO/eCRF) Clinical Trial Coordination and Data Management:  •  Recruitment and clinical management of stroke patients  •  Obtaining informed...
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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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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...
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Manpower Basel-Basel
and compliance of clinical trial materials across the global supply chain. The team provides QA oversight for the global IMP Distribution Network and works closely with key stakeholders in Global Clinical Supply Chain Management Distribution. This position offers...
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F. Hoffmann-La Roche AG-Basel
Scientists in a line‑ or functional‑manager capacity.  •  Interface closely with project team leaders and cross‑functional groups including safety, clinical pharmacology, clinical operations, biostatistics, regulatory, research, and biomarker teams.  •  Manage...
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Manpower Basel-Basel
Team: 7 people  •  Department: IMP Quality Distribution  •  Working hours: standard working hours Background IMP Quality Distribution is part of Global Quality Assurance and is responsible for maintaining the quality and compliance of clinical trial...
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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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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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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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Stiftung Weizenkorn-Basel
and be an active member of the Global Program Team (GPT), Global Clinical Team (GCT) and Clinical Trial Team (CTT) – responsible for safety issue management from formation of Global Program Team through Life Cycle Management  •  Responsible for overall signal...
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Manpower Basel-Basel
and provide scientific input into study management, signal evaluation, benefit-risk assessments, regulatory submissions and risk management activities. The position requires a strong understanding of drug safety, clinical development and regulated GxP...
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Swisslinx AG-Zurich
Minimum 2–3 years of experience in pharmacovigilance, medical writing, scientific editing or document quality review within the pharmaceutical or biotechnology industry. Strong understanding of pharmacovigilance, clinical trial safety, post-marketing...
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