Clinical Trial Manager Jobs
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Search Results - Clinical Trial Manager Jobs
Randstad (Schweiz) AG-Lausanne
execution in line 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...
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Nextrials, Inc.-Basel
the future of clinical development.
We are currently seeking a Senior Clinical Research Associate (CRA) to join our diverse and dynamic team. As a Senior CRA at ICON Plc, you will play a critical role in overseeing and managing clinical trial activities...
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Novocure Inc.-Baar
leading global clinical trials or overseeing international clinical study programs across multiple regions
• Previous experience leading physician teams and managing direct reports (Senior Director level)
• Strong understanding of the clinical...
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满天星人力资源管理有限公司-Basel
Responsibilities
Take overall ownership of formulating comprehensive strategies for Qilu Pharmaceutical's European clinical projects, including clinical development pathway planning, trial design optimization, and risk control. Ensure projects meet...
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Randstad (Schweiz) AG-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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Genentech-Kaiseraugst
with the people we love. That’s what makes us Roche.
The Production Enablement function ensures that packaging operations can produce material required by Roche’s clinical trials seamlessly, on-time, and while optimizing cost/quality. Leaders within...
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Debiopharm-Lausanne
and Clinical Data Management functions
• Proven expertise in clinical and pharmaceutical industry experience in planning and conducting clinical trials, preferably in early phase clinical development oncology studies within a pharmaceutical industry setting...
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Aenova Group / SwissCo Services AG-Sisseln
f/m/d)
Your key responsibilities
Supervision, organization, and coordination of the manufacture of preclinical trials as well as clinical investigational medicinal products (IMPs) in development projects in accordance with the applicable GMP guidelines...
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GlaxoSmithKline-Schweiz
that patient insights, lived experience, and priorities are systematically integrated into clinical development decision‑making, clinical trial design and execution, global medical strategy, and global product strategy.
This creates continuity between early...
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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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Aenova Group / SwissCo Services AG-Sisseln
key responsibilitiesSupervision, organization, and coordination of the manufacture of preclinical trials as well as clinical investigational medicinal products (IMPs) in development projects in accordance with the applicable GMP guidelinesSupervision...
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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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Discover International-Zurich
strategy for oncology programmes, with a focus on solid tumours and targeted therapies
Provide oversight for oncology clinical trial design, protocols, and study execution
Act as senior medical lead for safety review, clinical data interpretation...
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Aenova Group / SwissCo Services AG-Sisseln
Your key responsibilities
• Supervision, organization, and coordination of the manufacture of preclinical trials as well as clinical investigational medicinal products (IMPs) in development projects in accordance with the applicable GMP guidelines...
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CSL (EMEA)-Bern
The Associate Director (AD), Biostatistics, leads the full scope of statistical contribution to a clinical development program. The AD provides statistical strategies for the clinical trials and regulatory submissions, and is accountable...
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