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Clinical Trial Manager Jobs

1 - 15 of 64
1 - 15 of 64
Search Results - Clinical Trial Manager Jobs
CTC Resourcing Solutions-Basel
Clinical Development (CD) stakeholders Generates study metrics and status reports Represents Data Management (Biometry) at Clinical Trial Team (CTT) meetings, investigators and monitors meetings. Provides Data Management input to the development...
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Octapharma AG-Lachen
Clinical Trial Associate 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 in the world, developing...
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CTC Resourcing Solutions-Basel
A bio-pharmaceutical company in Switzerland is seeking a Senior Trial Data Manager for a 12-month contract based in Basel. The successful candidate will manage data management activities for outsourced studies, coordinate documentation development...
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InGoedeBanen.nl-Lausanne
with relevant pharmaceutical standards. Responsibilities  •  Support the Clinical Project Manager(s) in study execution, including tracking study milestones and key deliverables  •  Maintain and manage the Trial Master File (TMF/eTMF), performing periodic...
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Acrostak (Schweiz) AG-Winterthur
of experience in clinical project management within the medical device or pharmaceutical industry.  •  Swiss work permit / European citizenship is a must.  •  Proven track record of managing multiple clinical trials simultaneously  •  Strong knowledge of Good Clinical...
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Randstad (Schweiz) AG-Lausanne
pharmaceuticalstandards. Responsibilities  •  Supportthe Clinical Project Manager(s) in study execution, includingtracking study milestones and keydeliverables  •  Maintain andmanage the Trial Master File (TMF/eTMF), performing periodiccompleteness and qualityreviews...
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Universität Bern-Bern
and evaluate methods to generate decision-oriented evidence. Core areas include:  •  Methodology of clinical trials and randomized real-world evidence  •  Pragmatic trials embedded in routine care  •  Integration of digital health and research infrastructure...
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InGoedeBanen.nl-Lausanne
role within the Nestlé Health Science Supply Operations team. This position is responsible for defined aspects of Investigational Medicinal Products (IMP), Investigational Nutritional Products (INP), Clinical Trial Materials (CTM), and ancillary...
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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-Zurich
This role is suited for early to mid-career professionals with experience in clinical trials and GCP-based quality environments. It is a hands-on specialist role without management responsibility. Responsibilities  •  Support clinical quality oversight...
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Bayer CropScience Limited-Basel
and site experience. Your Tasks and Responsibilities  •  Site Relationship Management  •  Build and sustain strong, collaborative relationships with clinical key accounts to ensure smooth operations and effective communication.  •  Act as the primary...
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gloor&lang AG-Zurich
This role is suited for early to mid-career professionals with experience in clinical trials and GCP-based quality environments. It is a hands-on specialist role without management responsibility. Responsibilities  •  Support clinical quality oversight...
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Nestlé SA-Lausanne
nutrition, or CRO settings)  •  Experience and proven impact in leading safety management in complex clinical trials, including issue management and regulatory frameworks of nutrition and medical nutrition  •  Expertise in preparation of clinical safety...
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Meet Recruitment-Lachen
CTA 182702 Posted: 05/01/2026  •  Competitive  •  Lachen Switzerland A growing pharmaceutical company in Switzerland is seeking a proactive and detail-oriented Clinical Trials Associate (CTA) to support the operational delivery of clinical development...
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Kantonsspital Aarau-Aarau
Forschungsprojekten und bringen Monitoring-Erfahrung mitSie haben eine Ausbildung oder Studium im Bereich des Gesundheitswesens oder der Naturwissenschaften absolviert und, idealerweise, eine Weiterbildung im Bereich der klinischen Forschung (z.B. CAS Clinical Trial...
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