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Clinical Trial Manager Jobs

1 - 15 of 139
1 - 15 of 139
Search Results - Clinical Trial Manager Jobs
Randstad-Lausanne
and company procedures. This role leads study‑level operational strategy and is accountable for day‑to‑day clinical trial delivery across assigned programs but may also operate at the program/life cycle management level for a given asset. The sCPM provides...
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Barrington James Limited-Zurich
A boutique CRO in Switzerland is searching for a Head of Clinical Operations to lead and scale clinical trial activities for oncology studies. This role involves direct collaboration with sponsors, managing clinical operations teams, ensuring...
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Randstad-Lausanne
A leading recruitment agency is seeking a Senior Clinical Project Manager for a role in Lausanne, Switzerland. The ideal candidate will have over 8 years of experience in managing pharmaceutical clinical trials, ensuring timely and compliant...
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Barrington James Limited-Zurich
to‑end delivery of oncology clinical trials from start‑up through close‑out.  •  Ensure effective oversight of study start‑up, regulatory submissions, site management, monitoring, and vendors.  •  Proactively identify and mitigate risks specific to oncology...
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Randstad-Lausanne
a central role in startup activities, vendor selection and oversight, and cross-functional coordination. Although the position may involve line management and strategic clinical development planning responsibilities, the emphasis is on trial execution...
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CSL Behring AG-Bern
to lead strategic and operational CMC regulatory activities across product development, clinical submissions, registrations, and lifecycle management. In this role, you will shape global CMC regulatory strategy, ensure compliant execution...
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headcount-Zurich
and cross-functional decisions Requirements MSc or PhD in Life Sciences with 5+ years’ experience in Pharma / Biotech clinical project management Proven record managing early-phase trials and external partners (CROs / vendors) Solid knowledge of ICH-GCP...
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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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CSL Behring AG-Bern
to lead strategic and operational CMC regulatory activities across product development, clinical submissions, registrations, and lifecycle management. In this role, you will shape global CMC regulatory strategy, ensure compliant execution...
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JCW Group-Basel
Clinical Ops, Data, Safety) Implement risk management and ensure regulatory compliance Track study deliverables and oversee project reporting Qualifications Proven experience managing Phase II–III trials, ideally in oncology, CNS, or immunology Strong...
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Elan Personal AG-Schweiz
Biosamle Management Operational Excellence Clinical Trial Support QA Metadata GCP Compliance jid85a4040a jit0103a jiy26a...
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headcount | recruitment driven by science-Basel
registration-track clinical trials for rare diseases. This role acts as a key member of the interdisciplinary development team, reporting directly to the Head of Clinical Development, with high visibility and hands‑on leadership responsibility across study...
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Roche-Kaiseraugst
Distribution organisation’s objective is to cost-effectively ensure the right product is in the right place at the right time every time, such that no patient will go without treatment and no clinical trial will be delayed. The System & Process Chapter ensures...
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roche.com -
Matterhorn Biosciences AG-Basel
execution/conduct and report of Ph1/2 clinical trials in I&I space  •  Contribute to medical leadership team and clinical development strategy  •  Provide guidance and expertise in the development of clinical trial protocols and further study relevant...
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Daiichi Sankyo-Zurich
in the relevant therapeutic area is of advantage.  •  Good knowledge and experience in managing scientific studies and medical projects.  •  Good knowledge of clinical trial methodology is preferred.  •  Good understanding of applicable regulations, including...
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